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EUROPEAN JOURNAL OF NEUROLOGY,
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Sailer, A.
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UCL Inst Neurol, London, England UCL Inst Neurol, London, England

Scholz, S. W.
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h-index: 0
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NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA
Georgetown Univ, Dept Neurosci, Washington, DC USA UCL Inst Neurol, London, England

Gibbs, J. R.
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h-index: 0
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NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA UCL Inst Neurol, London, England

Johnson, J. O.
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h-index: 0
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NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA UCL Inst Neurol, London, England

Wood, N. W.
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h-index: 0
机构:
UCL Inst Neurol, London, England UCL Inst Neurol, London, England

Hernandez, D.
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h-index: 0
机构:
NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA UCL Inst Neurol, London, England

Hardy, J.
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h-index: 0
机构:
UCL Inst Neurol, London, England UCL Inst Neurol, London, England

Federoff, H.
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h-index: 0
机构:
Georgetown Univ, Dept Neurosci, Washington, DC USA UCL Inst Neurol, London, England

Traynor, B. J.
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h-index: 0
机构:
NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA UCL Inst Neurol, London, England

Singleton, A. B.
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h-index: 0
机构:
NIA, Neurogenet Lab, NIH, Bethesda, MD 20892 USA UCL Inst Neurol, London, England

Houlden, H.
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Impact of the metabolic syndrome on atrial size in patients with new-onset atrial fibrillation
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Nicolaou, Vasilios N.
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Papadakis, John E.
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Hellen Red Cross Hosp, Cardiol Dept 1, Athens, Greece Hellen Red Cross Hosp, Cardiol Dept 1, Athens, Greece

Karatzis, Emmanouil N.
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Dermitzaki, Sofia I.
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Hellen Red Cross Hosp, Cardiol Dept 1, Athens, Greece Hellen Red Cross Hosp, Cardiol Dept 1, Athens, Greece

Tsakiris, Alexandros K.
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Hellen Red Cross Hosp, Cardiol Dept 1, Athens, Greece Hellen Red Cross Hosp, Cardiol Dept 1, Athens, Greece

Skoufas, Panagiotis D.
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Loi, S.
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Kwak, Soo Heon
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Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Jung, Chan-hyeon
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Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Ahn, Chang Ho
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h-index: 0
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Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea
Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Park, Jungsun
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SK Telecom, New Business Div, Seongnam, Gyeonggi Do, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Chae, Jeesoo
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Seoul Natl Univ, Coll Med, Dept Biomed Sci, Seoul, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Jung, Hye Seung
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Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Cho, Young Min
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Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea
Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Lee, Dae Ho
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Gachon Univ, Gil Med Ctr, Dept Internal Med, Inchon, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Kim, Jong-Il
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Seoul Natl Univ, Coll Med, Dept Biomed Sci, Seoul, South Korea Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea

Park, Kyong Soo
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Seoul Natl Univ Hosp, Dept Internal Med, 101 Daehak Ro, Seoul 03080, South Korea
Seoul Natl Univ, Coll Med, Dept Internal Med, Seoul, South Korea
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Homma, Thais Kataoka
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Homma, Thais Kataoka
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h-index: 0
机构:
FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil
FMUSP, Hosp Clin Fac, Dev Endocrinol Unit, Lab Hormones & Mol Genet LIM42, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Freire, Bruna Lucheze
论文数: 0 引用数: 0
h-index: 0
机构:
FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil
FMUSP, Hosp Clin Fac, Dev Endocrinol Unit, Lab Hormones & Mol Genet LIM42, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Honjo Kawahira, Rachel Sayuri
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h-index: 0
机构:
Univ Sao Paulo, Hosp Clin, Inst Crianca, Fac Med,Genet Unit, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Dauber, Andrew
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h-index: 0
机构:
Childrens Natl Hlth Syst, Div Endocrinol, Washington, DC USA FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

de Assis Funari, Mariana Ferreira
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h-index: 0
机构:
FMUSP, Hosp Clin Fac, Dev Endocrinol Unit, Lab Hormones & Mol Genet LIM42, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

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Nishi, Mirian Yumie
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FMUSP, Hosp Clin Fac, Dev Endocrinol Unit, Lab Hormones & Mol Genet LIM42, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

de Albuquerque, Edoarda Vasco
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h-index: 0
机构:
FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Vasques, Gabriela de Andrade
论文数: 0 引用数: 0
h-index: 0
机构:
FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Collett-Solberg, Paulo Ferrez
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h-index: 0
机构:
Univ Estado Rio de Janeiro, Fac Ciencia Med, Endocrinol Discipline, Rio De Janeiro, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Miura Sugayama, Sofia Mizuho
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Hosp Clin, Inst Crianca, Fac Med,Genet Unit, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Bertola, Debora Romeo
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Hosp Clin, Inst Crianca, Fac Med,Genet Unit, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Kim, Chong Ae
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Sao Paulo, Hosp Clin, Inst Crianca, Fac Med,Genet Unit, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Prado Arnhold, Ivo Jorge
论文数: 0 引用数: 0
h-index: 0
机构:
FMUSP, Hosp Clin Fac, Dev Endocrinol Unit, Lab Hormones & Mol Genet LIM42, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

Malaquias, Alexsandra Christianne
论文数: 0 引用数: 0
h-index: 0
机构:
FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil
Fac Ciencias Med Santa Casa Sao Paulo, Irmandade Santa Casa Misericordia Sao Paulo, Dept Pediat, Pediat Endocrinol Unit, Sao Paulo, SP, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil

de Lima Jorge, Alexander Augusto
论文数: 0 引用数: 0
h-index: 0
机构:
FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil
FMUSP, Hosp Clin Fac, Dev Endocrinol Unit, Lab Hormones & Mol Genet LIM42, Sao Paulo, Brazil FMUSP, Hosp Clin, Genet Endocrinol Unit, Lab Cellular & Mol Endocrinol LIM25, Sao Paulo, Brazil
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Aaltio, Juho
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Hyttinen, Virva
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Lonnqvist, Tuula
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Isohanni, Pirjo
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EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY,
2022, 36
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Aaltio, Juho
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h-index: 0
机构:
Univ Helsinki, Res Programs Unit, Stem Cells & Metab, Helsinki, Finland Univ Helsinki, Res Programs Unit, Stem Cells & Metab, Helsinki, Finland

Hyttinen, Virva
论文数: 0 引用数: 0
h-index: 0
机构:
VATT Inst Econ Res, Helsinki, Finland
Univ Eastern Finland, Dept Hlth & Social Management, Kuopio, Finland Univ Helsinki, Res Programs Unit, Stem Cells & Metab, Helsinki, Finland

Kortelainen, Mika
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h-index: 0
机构:
VATT Inst Econ Res, Helsinki, Finland
Turku Sch Econ & Business Adm, Dept Econ, Turku, Finland Univ Helsinki, Res Programs Unit, Stem Cells & Metab, Helsinki, Finland

Frederix, Gerardus W. J.
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h-index: 0
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Univ Med Ctr, Dept Genet, Utrecht, Netherlands
Univ Med Ctr, Julius Ctr Hlth Sci & Primary Care, Utrecht, Netherlands Univ Helsinki, Res Programs Unit, Stem Cells & Metab, Helsinki, Finland

Lonnqvist, Tuula
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h-index: 0
机构:
Univ Helsinki, Childrens Hosp, Pediat Res Ctr, Dept Child Neurol, Helsinki, Finland
Helsinki Univ Hosp, Helsinki, Finland Univ Helsinki, Res Programs Unit, Stem Cells & Metab, Helsinki, Finland

Suomalainen, Anu
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h-index: 0
机构:
Univ Helsinki, Res Programs Unit, Stem Cells & Metab, Helsinki, Finland
Helsinki Univ Hosp, HUS Diagnost, Helsinki, Finland Univ Helsinki, Res Programs Unit, Stem Cells & Metab, Helsinki, Finland

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Clinical Utility of Rapid Exome Sequencing Combined With Mitochondrial DNA Sequencing in Critically Ill Pediatric Patients With Suspected Genetic Disorders
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Ouyang, Xuejun
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Zhang, Yu
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2021, 12

Ouyang, Xuejun
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h-index: 0
机构:
Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Zhang, Yu
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h-index: 0
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Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Zhang, Lijuan
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h-index: 0
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Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Luo, Jixuan
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h-index: 0
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Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Zhang, Ting
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h-index: 0
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Shanghai Childrens Hosp, Dept Gastroenterol, Shanghai, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Hu, Hui
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h-index: 0
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Shanghai Childrens Hosp, Dept Gastroenterol, Shanghai, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Liu, Lin
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h-index: 0
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Guangdong Prov Peoples Hosp, Dept Vasculocardiol, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Zhong, Lieqiang
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h-index: 0
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Guangdong Prov Peoples Hosp, Dept Vasculocardiol, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Zeng, Shaoying
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h-index: 0
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Guangdong Prov Peoples Hosp, Dept Vasculocardiol, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Xu, Pingyi
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h-index: 0
机构:
Guangzhou Med Univ, Affiliated Hosp 1, Dept Neurol, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Bai, Zhenjiang
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h-index: 0
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Soochow Univ, Childrens Hosp, Dept Crit Care Med, Suzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Wong, Lee-Jun
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h-index: 0
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Baylor Coll Med, Dept Human & Mol Genet, Houston, TX 77030 USA Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Wang, Jing
论文数: 0 引用数: 0
h-index: 0
机构:
Baylor Coll Med, Dept Human & Mol Genet, Houston, TX 77030 USA
AmCare Genom Lab, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Wang, Chunli
论文数: 0 引用数: 0
h-index: 0
机构:
AmCare Genom Lab, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Wang, Bin
论文数: 0 引用数: 0
h-index: 0
机构:
Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China

Zhang, Victor Wei
论文数: 0 引用数: 0
h-index: 0
机构:
Baylor Coll Med, Dept Human & Mol Genet, Houston, TX 77030 USA
AmCare Genom Lab, Guangzhou, Peoples R China Southern Med Univ, Zhujiang Hosp, Dept Pediat, Guangzhou, Peoples R China
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The diagnostic rate of inherited metabolic disorders by exome sequencing in a cohort of 547 individuals with developmental disorders
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Delanne, Julian
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Bruel, Ange-Line
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Huet, Frederic
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Moutton, Sebastien
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Nambot, Sophie
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Grisval, Margot
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Houcinat, Nada
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Kuentz, Paul
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Sorlin, Arthur
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Callier, Patrick
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Jean-Marcais, Nolwenn
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Mosca-Boidron, Anne-Laure
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Mau-Them, Frederic Tran
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Denomme-Pichon, Anne-Sophie
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Vitobello, Antonio
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Lehalle, Daphne
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El Chehadeh, Salima
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Francannet, Christine
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Lebrun, Marine
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Lambert, Laetitia
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Jacquemont, Marie-Line
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Gerard-Blanluet, Marion
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Alessandri, Jean-Luc
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Willems, Marjolaine
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Thevenon, Julien
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Chouchane, Mondher
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Darmency, Veronique
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Fatus-Fauconnier, Clemence
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Gay, Sebastien
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Bournez, Marie
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Masurel, Alice
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Leguy, Vanessa
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Duffourd, Yannis
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Philippe, Christophe
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Feillet, Francois
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Faivre, Laurence
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Thauvin-Robinet, Christel
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MOLECULAR GENETICS AND METABOLISM REPORTS,
2021, 29

Delanne, Julian
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Bruel, Ange-Line
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Huet, Frederic
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Moutton, Sebastien
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Nambot, Sophie
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Grisval, Margot
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Houcinat, Nada
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Kuentz, Paul
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France
CHU Besancon, Biol Mol, Besancon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Sorlin, Arthur
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Callier, Patrick
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Cytogenet & Genet Mol, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Jean-Marcais, Nolwenn
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Mosca-Boidron, Anne-Laure
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Lab Cytogenet & Genet Mol, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Mau-Them, Frederic Tran
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Denomme-Pichon, Anne-Sophie
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Vitobello, Antonio
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Lehalle, Daphne
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

El Chehadeh, Salima
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Francannet, Christine
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Clermont Ferrand, Ctr Reference Deficiences Intellectuelles Causes, Serv Genet Med, Clermont Ferrand, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Lebrun, Marine
论文数: 0 引用数: 0
h-index: 0
机构:
CHU St Etienne, Lab Genet, St Etienne, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Lambert, Laetitia
论文数: 0 引用数: 0
h-index: 0
机构:
CHRU Nancy, Serv Genet Clin, Nancy, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Jacquemont, Marie-Line
论文数: 0 引用数: 0
h-index: 0
机构:
CHU La Reunion, Grp Hosp Sud Reunion, Unite Genet Med, Pole Femme Mere Enfant, St Pierre, Reunion, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Gerard-Blanluet, Marion
论文数: 0 引用数: 0
h-index: 0
机构:
Robert Debre Hosp, AP HP, Dept Genet, Paris, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Alessandri, Jean-Luc
论文数: 0 引用数: 0
h-index: 0
机构:
CHU La Reunion, CH Felix Guyon, Serv Reanimat Neonatale, Pole Femme Mere Enfant, St Denis, Reunion, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Willems, Marjolaine
论文数: 0 引用数: 0
h-index: 0
机构:
Arnaud Villeneuve Hosp, Reference Ctr Rare Dis Dev Disorders & Multiple C, Dept Med Genet, Montpellier, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Thevenon, Julien
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Chouchane, Mondher
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Darmency, Veronique
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Fatus-Fauconnier, Clemence
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Gay, Sebastien
论文数: 0 引用数: 0
h-index: 0
机构:
CH William Morey, Serv Pediat, Chalon Sur Saone, Saone & Loire, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Bournez, Marie
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Masurel, Alice
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Leguy, Vanessa
论文数: 0 引用数: 0
h-index: 0
机构:
CHU Dijon Bourgogne, Ctr Competence Malad Hereditaires Metab, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Duffourd, Yannis
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Philippe, Christophe
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Feillet, Francois
论文数: 0 引用数: 0
h-index: 0
机构:
Arnaud Villeneuve Hosp, Reference Ctr Rare Dis Dev Disorders & Multiple C, Dept Med Genet, Montpellier, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Faivre, Laurence
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon, CHU Dijon Bourgogne, Ctr Reference Malad Rares Anomalies Dev & Syndrom, Ctr Genet,FHU TRANSLAD, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France

Thauvin-Robinet, Christel
论文数: 0 引用数: 0
h-index: 0
机构:
Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
CHU Dijon Bourgogne, Lab Genet Chromosom Mol, Unite Fonct dInnovat Diagnost Malad Rares, Dijon, France
CHU Dijon Bourgogne, Ctr Reference Malad Rares Deficiences Intellectue, Ctr Genet, FHU TRANSLAD, Dijon, France Univ Bourgogne Franche Comte, CHU Dijon Bourgogne, INSERM,FHU TRANSLAD, UMR 1231,GAD Team,Genet Dev Disorders, Dijon, France
[40]
METABOLIC ABNORMALITIES AND NEW-ONSET SEIZURES IN HUMAN IMMUNODEFICIENCY VIRUS-SEROPOSITIVE PATIENTS
[J].
VANPAESSCHEN, W
;
BODIAN, C
;
MAKER, H
.
EPILEPSIA,
1995, 36 (02)
:146-150

VANPAESSCHEN, W
论文数: 0 引用数: 0
h-index: 0
机构: BETH ISRAEL MED CTR, DEPT NEUROL, NEW YORK, NY 10003 USA

BODIAN, C
论文数: 0 引用数: 0
h-index: 0
机构: BETH ISRAEL MED CTR, DEPT NEUROL, NEW YORK, NY 10003 USA

MAKER, H
论文数: 0 引用数: 0
h-index: 0
机构: BETH ISRAEL MED CTR, DEPT NEUROL, NEW YORK, NY 10003 USA