Results 171 to 180 of about 87,754 (311)

Parental age and risk of genetic syndromes predisposing to nervous system tumors: nested case–control study

Clinical Epidemiology, 2018
Maral Adel Fahmideh,1 Giorgio Tettamanti,1 Catharina Lavebratt,2 Mats Talbäck,1 Tiit Mathiesen,3,4 Birgitta Lannering,5 Kimberly J Johnson,6,7 Maria Feychting1 1Unit of Epidemiology, Institute of Environmental Medicine, Karolinska Institutet ...
Adel Fahmideh M, Tettamanti G, Lavebratt C, Talbäck M, Mathiesen T, Lannering B, Johnson KJ, Feychting M   +7 more
doaj  

Updated nomenclature for human and mouse neurofibromatosis type 1 genes [PDF]

, 2017
Anastasaki, Corina, Gutmann, David H, Kesterson, Robert A, Le, Lu Q   +3 more
core   +2 more sources

RECKLINGHAUSEN'S DISEASE IN А PREGNANT WOMAN: A CLINICAL CASE

Мать и дитя в Кузбассе
Recklinghausen's disease (neurofibromatosis) was first described in 1882. Neurofibromatosis (non-malignant) is classified as a phacomatosis according to the International Classification of Diseases X revision (Q85.0) and is included in the list of orphan
Владимир Кириллович Чайка, Ирина Тихоновна Говоруха, Виталина Васильевна Вустенко, Арина Александровна Земелько   +3 more
doaj  

Leprosy with neurofibromatosis – a diagnostic dilemma

, 2005
Chander Grover, Manmohan Lohra, Soni Nanda, B. S. N. Reddy   +3 more
openalex   +1 more source

Calvarial defects and Dandy-Walker malformation in association with neurofibromatosis type 1 [PDF]

, 2014
Na Meng, Chuncheng Xie, Haiyang Wang, Hong Shen, Zhiguo Lin   +4 more
openalex   +1 more source

Neurofibromatosis type 1

, 2021
Mahesh Gautam
openalex   +1 more source

Simultaneous Moyamoya disease and cervical spinal cord low-grade astrocytoma in a child with neurofibromatosis type 1 [PDF]

, 2013
Jeffrey J. Gold, Chris E Dory, Michael L. Levy, John R. Crawford   +3 more
openalex   +1 more source

Neurofibromatosis Type 1: Optimizing Management with a Multidisciplinary Approach

Journal of Multidisciplinary Healthcare
Shaan Lalvani, Rebecca M Brown Department of Neurology, The Mount Sinai Hospital, New York, NY, USACorrespondence: Rebecca M Brown, MD, PhD, The Mount Sinai Hospital, Department of Neurology, 1216 5th Avenue, New York, NY, 10029, USA, Tel +1 2128248579 ...
Lalvani S, Brown RM
doaj  

Oncogenetic testing, diagnosis and follow-up in Birt-Hogg-Dubé syndrome, familial atypical multiple mole melanoma syndrome and neurofibromatosis 1 and 2 [PDF]

, 2015
't Kint de Roodenbeke, Daphné, Baurain, Jean-François, Brochez, Lieve, Caplanusi, Teofila, Claes, Kathleen, Hulstaert, Frank, Legius, Eric, Poppe, Bruce, Robays, Jo, Rottey, Sylvie, Schrijvers, Dirk, Stordeur, Sabine, Ullman, Urielle, Van Maerken, Tom   +13 more
core  

Prenatal diagnosis and hemodynamic evaluation of Klippel-Trenaunay-Weber syndrome. [PDF]

, 1998
CAPUANO P, D'ARMIENTO, MARIA, LAMBERTI A, LIGUORI M, MARTINELLI, PASQUALE, PALADINI, DARIO, TEODORO A   +6 more
core   +1 more source