Clinical and Mutational Spectrum of Neurofibromatosis Type 1-like Syndrome (vol 302, pg 2111, 2009)

被引：1

作者：

Messiaen, Ludwine

机构：

来源：

JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION | 2010年 / 303卷 / 24期

关键词：

D O I：

10.1001/jama.2010.828

中图分类号：

R5 [内科学];

学科分类号：

1002 ; 100201 ;

摘要：

引用

页码：2477 / 2477

页数：1

共 50 条

[41] Sirolimus for progressive neurofibromatosis type 1-associated plexiformneurofibromas: a Neurofibromatosis Clinical Trials Consortium phase II study (vol 17, pg 596, 2015)
Weiss
NEURO-ONCOLOGY, 2015, 17 (06) : 905 - 905
[42] The Validity and Clinical Utility of Night Eating Syndrome (vol 42, pg 720, 2009)
Striegel-Moore, Ruth H.
Franko, Debra L.
Garcia, Jennifer
INTERNATIONAL JOURNAL OF EATING DISORDERS, 2011, 44 (01) : 94 - 94
[43] Regarding "Vascular abnormalities in patients with neurofibromatosis syndrome type I: Clinical spectrum, management, and results" - Reply
Oderich, Gustavo S.
JOURNAL OF VASCULAR SURGERY, 2008, 47 (06) : 1379 - 1379
[44] Clinical Care in the Aging Century: Announcing "Care of the Aging Patient: From Evidence to Action" (vol 302, pg 2703, 2009)
Landefeld, C. S.
Winker, M. A.
Chernof, B.
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2010, 303 (05): : 422 - 422
[45] Prevalence of neurofibromatosis type 1 in congenital pseudarthrosis of the tibia (vol 175, pg 1193, 2016)
Van Royen, Kjell
Brems, Hilde
Legius, Eric
Lammens, Johan
Laumen, Armand
EUROPEAN JOURNAL OF PEDIATRICS, 2017, 176 (07) : 993 - 993
[46] Gastrointestinal juvenile-like (inflammatory/hyperplastic) mucosal polyps in neurofibromatosis type 1 with no concurrent genetic or clinical evidence of other syndromes (vol 474, pg 259, 2018)
Ravegnini, Gloria
Quero, Giuseppe
Sammarini, Giulia
Giustiniani, Maria Cristina
Castri, Federica
Pomponi, Maria Grazia
Angelini, Sabrina
Alfieri, Sergio
Genuardi, Maurizio
Zamboni, Giuseppe
Ricci, Riccardo
VIRCHOWS ARCHIV, 2019, 474 (02) : 265 - 265
[47] Mutation Spectrum of NF1 and Clinical Characteristics in 78 Korean Patients With Neurofibromatosis Type 1
Ko, Jung Min
Sohn, Young Bae
Jeong, Seon Yong
Kim, Hyon-Ju
Messiaen, Ludwine M.
PEDIATRIC NEUROLOGY, 2013, 48 (06) : 447 - 453
[48] CREBBP and EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein-Taybi syndrome EP300 mutational spectrum and clinical presentations in a cohort of Swedish patients with Rubinstein-Taybi syndrome (vol 4, pg 39, 2016)
Wincent, Josephine
Luthman, Aron
van Belzen, Martine
van der Lans, Christian
Albert, Johanna
Nordgren, Ann
Anderlid, Britt-Marie
MOLECULAR GENETICS & GENOMIC MEDICINE, 2016, 4 (03): : 367 - 367
[49] PROTON MR SPECTROSCOPY IN PATIENTS WITH NEUROFIBROMATOSIS TYPE-1 - EVALUATION OF HAMARTOMAS AND CLINICAL CORRELATION (VOL 16, PG 141, 1995)
CASTILLO
AMERICAN JOURNAL OF NEURORADIOLOGY, 1995, 16 (04) : 808 - 808
[50] Aicardi-Goutieres Syndrome Type 1: A Novel Missense Variant and Review of the Mutational Spectrum
Tasharrofi, Behnoosh
Karimzadeh, Parvaneh
Asadollahi, Mostafa
Hasani, Sepideh
Heidari, Morteza
Keramatipour, Mohammad
IRANIAN JOURNAL OF CHILD NEUROLOGY, 2024, 18 (03) : 117 - 129

← 1 2 3 4 5 →