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- [1] Non-immune Hydrops Fetalis and Generalized Lymphatic Dysplasia Associated With PIEZO1 MutationsAMERICAN JOURNAL OF RESPIRATORY AND CRITICAL CARE MEDICINE, 2024, 209Goncalves, A. J. Cabrera论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Jackson Mem Hosp, Pediat, Miami, FL USA Univ Miami, Jackson Mem Hosp, Pediat, Miami, FL USAVelez, C. Aguilar论文数: 0 引用数: 0 h-index: 0机构: Jackson Mem Hosp, Pediat, Miami, FL USA Univ Miami, Jackson Mem Hosp, Pediat, Miami, FL USACardenas, M. R.论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Pediat Pulmonol, Miami, FL USA Univ Miami, Jackson Mem Hosp, Pediat, Miami, FL USANieto, A. Heredia论文数: 0 引用数: 0 h-index: 0机构: Univ Miami, Jackson Mem Hosp, Pediat, Miami, FL USA Univ Miami, Jackson Mem Hosp, Pediat, Miami, FL USA
- [2] Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalisNature Communications, 6Elisavet Fotiou论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineSilvia Martin-Almedina论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineMichael A. Simpson论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineShin Lin论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineKristiana Gordon论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineGlen Brice论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineGiles Atton论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineIona Jeffery论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineDavid C. Rees论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineCyril Mignot论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineJulie Vogt论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineTessa Homfray论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineMichael P. Snyder论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineStanley G. Rockson论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineSteve Jeffery论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicinePeter S. Mortimer论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicineSahar Mansour论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular MedicinePia Ostergaard论文数: 0 引用数: 0 h-index: 0机构: Cardiovascular and Cell Sciences Institute,Department of Medical and Molecular Genetics, Division of Genetics and Molecular Medicine
- [3] Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalisNATURE COMMUNICATIONS, 2015, 6Fotiou, Elisavet论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandMartin-Almedina, Silvia论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandSimpson, Michael A.论文数: 0 引用数: 0 h-index: 0机构: Guys Hosp, Dept Med & Mol Genet, Div Genet & Mol Med, Kings Coll London,Sch Med, London SE1 9RY, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandLin, Shin论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Div Cardiovasc Med, Stanford, CA 94305 USA Stanford Univ, Dept Genet, Stanford, CA 94305 USA St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandGordon, Kristiana论文数: 0 引用数: 0 h-index: 0机构: St Georges Healthcare NHS Trust, Dept Dermatol, London SW17 0QT, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandBrice, Glen论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, South West Thames Reg Genet Unit, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandAtton, Giles论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, South West Thames Reg Genet Unit, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandJeffery, Iona论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, Dept Pathol, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandRees, David C.论文数: 0 引用数: 0 h-index: 0机构: Kings Coll Hosp London, Kings Coll London, Sch Med, Dept Haematol Med, London SE5 9RS, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandMignot, Cyril论文数: 0 引用数: 0 h-index: 0机构: GH Pitie Salpetriere, Ctr Reference Deficiences Intellectuelles Causes, Dept Genet, F-75013 Paris, France St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandVogt, Julie论文数: 0 引用数: 0 h-index: 0机构: Birmingham Womens Hosp, West Midlands Reg Genet Serv, Clin Genet Unit, Birmingham B15 2TG, W Midlands, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandHomfray, Tessa论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, South West Thames Reg Genet Unit, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandSnyder, Michael P.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Dept Genet, Stanford, CA 94305 USA St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandRockson, Stanley G.论文数: 0 引用数: 0 h-index: 0机构: Stanford Univ, Div Cardiovasc Med, Stanford, CA 94305 USA St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandJeffery, Steve论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandMortimer, Peter S.论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandMansour, Sahar论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, South West Thames Reg Genet Unit, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, EnglandOstergaard, Pia论文数: 0 引用数: 0 h-index: 0机构: St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, England St Georges Univ London, Cardiovasc & Cell Sci Inst, London SW17 0RE, England
- [4] Case Report: Whole Exome Sequencing Revealed Two Novel Mutations of PIEZO1 Implicated in Nonimmune Hydrops FetalisFRONTIERS IN GENETICS, 2021, 12Chen, Yuan论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaJiang, Ying论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaChen, Bangwu论文数: 0 引用数: 0 h-index: 0机构: Ninghai Maternal & Child Hlth Care Hosp, Dept Obstet, Ningbo, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaQian, Yeqing论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Dept Reprod Genet, Womens Hosp, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaLiu, Jiao论文数: 0 引用数: 0 h-index: 0机构: Lishui Maternal & Child Hlth Care Hosp, Dept Obstet, Lishui, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaYang, Mengmeng论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaZhao, Baihui论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R ChinaLuo, Qiong论文数: 0 引用数: 0 h-index: 0机构: Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China Zhejiang Univ, Womens Hosp, Dept Obstet, Sch Med, Hangzhou, Peoples R China
- [5] Identification of novel PIEZO1 variants using prenatal exome sequencing and correlation to ultrasound and autopsy findings of recurrent hydrops fetalisAMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2018, 176 (12) : 2829 - 2834Datkhaeva, Ilina论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAArboleda, Valerie A.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USASenaratne, T. Niroshi论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USANikpour, Gelareh论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAMeyerson, Cherise论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAGeng, Yipeng论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAAfshar, Yalda论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAScibetta, Emily论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAGoldstein, Jeffrey论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAQuintero-Rivera, Fabiola论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USACrandall, Barbara F.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Prenatal Diag Ctr, Dept Psychiat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAGrody, Wayne W.论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Human Genet, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USADeignan, Joshua论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, UCLA Clin Genom Ctr, Dept Pathol & Lab Med, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USAJanzen, Carla论文数: 0 引用数: 0 h-index: 0机构: Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA Univ Calif Los Angeles, David Geffen Sch Med, Dept Obstet & Gynecol, Los Angeles, CA 90095 USA
- [6] Author Correction: Novel mutations in PIEZO1 cause an autosomal recessive generalized lymphatic dysplasia with non-immune hydrops fetalisNature Communications, 10Elisavet Fotiou论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteSilvia Martin-Almedina论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteMichael A. Simpson论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteShin Lin论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteKristiana Gordon论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteGlen Brice论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteGiles Atton论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteIona Jeffery论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteDavid C. Rees论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteCyril Mignot论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteJulie Vogt论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteTessa Homfray论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteMichael P. Snyder论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteStanley G. Rockson论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteSteve Jeffery论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstitutePeter S. Mortimer论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstituteSahar Mansour论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences InstitutePia Ostergaard论文数: 0 引用数: 0 h-index: 0机构: St. George’s University of London,Cardiovascular and Cell Sciences Institute
- [7] PIEZO1 is the most common monogenic etiology of non-immune hydrops fetalis detected by prenatal exome sequencingPRENATAL DIAGNOSIS, 2023, 43 (12) : 1556 - 1566Brewer, Casey J.论文数: 0 引用数: 0 h-index: 0机构: Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USA Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USAMakhamreh, Mona M.论文数: 0 引用数: 0 h-index: 0机构: Maimonides Hosp, Dept Obstet & Gynecol, Brooklyn, NY USA Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USAShivashankar, Kavya论文数: 0 引用数: 0 h-index: 0机构: Univ Chicago, Dept Obstet & Gynecol, Chicago, IL USA Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USAMcLaren, Rodney论文数: 0 引用数: 0 h-index: 0机构: Thomas Jefferson Univ, Sidney Kimmel Med Coll, Div Maternal Fetal Med, 833 Chestnut St, Philadelphia, PA 19107 USA Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USAToro, Mariella论文数: 0 引用数: 0 h-index: 0机构: Thomas Jefferson Univ, Sidney Kimmel Med Coll, Philadelphia, PA 19107 USA Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USABerger, Seth I.论文数: 0 引用数: 0 h-index: 0机构: Childrens Natl Med Ctr, Rare Dis Inst, Ctr Genet Med Res, Washington, DC USA Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USAAl-Kouatly, Huda B.论文数: 0 引用数: 0 h-index: 0机构: Thomas Jefferson Univ, Sidney Kimmel Med Coll, Div Maternal Fetal Med, 833 Chestnut St, Philadelphia, PA 19107 USA Cincinnati Childrens Hosp Med Ctr, Div Human Genet, Cincinnati, OH USA
- [8] Perinatal presentations of non-immune hydrops fetalis due to recessive PIEZO1 disease: A challenging fetal diagnosisCLINICAL GENETICS, 2023, 103 (05) : 560 - 565Ghesh, Leila论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, UF Foetopathol & Genet 9321, Nantes, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceDesir, Julie论文数: 0 引用数: 0 h-index: 0机构: Clin Univ Bruxelles, Serv Genet Med, Hop Erasme, Brussels, Belgium CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceHaye, Damien论文数: 0 引用数: 0 h-index: 0机构: Hosp Civils Lyon, Serv Genet Med, Lyon, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceLe Tanno, Pauline论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble, Dept Genet & Procreat, Hop Couple Enfant, Grenoble, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceDevillard, Francoise论文数: 0 引用数: 0 h-index: 0机构: CHU Grenoble, Dept Genet & Procreat, Hop Couple Enfant, Grenoble, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceCogne, Benjamin论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, UF Foetopathol & Genet 9321, Nantes, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceMarangoni, Martina论文数: 0 引用数: 0 h-index: 0机构: Clin Univ Bruxelles, Lab Genet Mol, Hop Erasme, Brussels, Belgium CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceTecco, Laura论文数: 0 引用数: 0 h-index: 0机构: Ctr Hosp Univ St Pierre, Serv Gynecol Obstet, Brussels, Belgium CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceHeron, Delphine论文数: 0 引用数: 0 h-index: 0机构: Hop Univ Pitie Salpetriere Charles Foix, Ctr Reference Deficiences Intellectuelles, Serv Genet Med, Paris, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceLe Vaillant, Claudine论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, Serv Gynecol Obstet, Diagnost Antenatal, Nantes, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceJoubert, Madeleine论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, UF Foetopathol & Genet 9321, Nantes, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, FranceBeneteau, Claire论文数: 0 引用数: 0 h-index: 0机构: CHU Nantes, UF Foetopathol & Genet 9321, Nantes, France CHU Nantes, UF Foetopathol & Genet 9321, Nantes, France
- [9] Non-immune hydrops fetalis caused by PIEZO1 compound heterozygous deletions detected only by exome sequencingPRENATAL DIAGNOSIS, 2022, 42 (07) : 890 - 893Reytan, Sivan论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genom Ctr, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, IsraelHenig, Noa Zunz论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genom Ctr, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, IsraelYinon, Yoav论文数: 0 引用数: 0 h-index: 0机构: Sheba Med Ctr, Dept Obstet & Gynecol, Fetal Med Unit, Ramat Gan, Israel Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, IsraelAvnet, Hagai论文数: 0 引用数: 0 h-index: 0机构: Sheba Med Ctr, Dept Obstet & Gynecol, Fetal Med Unit, Ramat Gan, Israel Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, IsraelKurolap, Alina论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genom Ctr, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, IsraelYaron, Yuval论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genom Ctr, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, IsraelFeldman, Hagit Baris论文数: 0 引用数: 0 h-index: 0机构: Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genom Ctr, Weitzman 6, IL-6423960 Tel Aviv, Israel Tel Aviv Univ, Sackler Fac Med, Tel Aviv, Israel Tel Aviv Sourasky Med Ctr, Genet Inst, Weitzman 6, IL-6423960 Tel Aviv, Israel
- [10] Recurrent Nonimmune Fetal Hydrops Due to a Novel Pathogenic Variant in PIEZO1 Gene: A Case Report from South IndiaJOURNAL OF FETAL MEDICINE, 2023, 10 (02) : 69 - 72Nair, Lekshmi Sivaraman论文数: 0 引用数: 0 h-index: 0机构: NIMS Medicity, Dept Clin Genet, Trivandrum, Kerala, India NIMS Medicity, Dept Clin Genet, Trivandrum 695121, Kerala, India NIMS Medicity, Dept Clin Genet, Trivandrum, Kerala, IndiaDubey, Aditi论文数: 0 引用数: 0 h-index: 0机构: ARMC Aegis Hosp, Dept Fetal Med, Perinthlamanna, Kerala, India NIMS Medicity, Dept Clin Genet, Trivandrum, Kerala, IndiaMohan, Nisha论文数: 0 引用数: 0 h-index: 0机构: ARMC Aegis Hosp, Dept Clin Genet, Perinthlamanna, Kerala, India NIMS Medicity, Dept Clin Genet, Trivandrum, Kerala, IndiaVikraman, Seneesh Kumar论文数: 0 引用数: 0 h-index: 0机构: ARMC Aegis Hosp, Dept Fetal Med, Perinthlamanna, Kerala, India NIMS Medicity, Dept Clin Genet, Trivandrum, Kerala, IndiaDesai, Jay论文数: 0 引用数: 0 h-index: 0机构: ARMC Aegis Hosp, Dept Clin Genet, Perinthlamanna, Kerala, India NIMS Medicity, Dept Clin Genet, Trivandrum, Kerala, IndiaMadadi, Manasa论文数: 0 引用数: 0 h-index: 0机构: ARMC Aegis Hosp, Dept Clin Genet, Perinthlamanna, Kerala, India NIMS Medicity, Dept Clin Genet, Trivandrum, Kerala, India