Results 191 to 200 of about 27,346,886 (339)

Mosaic neurofibromatosis type 1

, 2008
Christine Liang, Julie V. Schaffer
openalex   +2 more sources

A rare case of patient with neurofibromatosis type 1 in a genotype–phenotype correlation revealing a submicroscopic deletion on the long arm of chromosome 17

, 2021
Yethindra Vityala, Tugolbai Tagaev, Elmira Mamytova, Elmira Mainazarova, Cholpon Dzhumakova, Asel Namazbekova   +5 more
openalex   +1 more source

Neurofibromatosis Type 1 with Neck and Thoraco-Abdominal Involvement: A Case Series Showing Different Localization and MRI Features

, 2021
Silvia Tortora, Andrea Esposito, Gianmarco Della Pepa, Michele Paternò, Giulia Cagnoli, Claudia Cesaretti, Federica Natacci, Gianpaolo Carrafiello   +7 more
openalex   +2 more sources

Endocrine Implications of Neurofibromatosis 1 in Childhood

Hormone Research in Paediatrics, 2015
C. Bizzarri, G. Bottaro
semanticscholar   +1 more source

Healthcare utilization patterns and costs related to neurofibromatosis 1 in Ontario, Canada. [PDF]

Orphanet J Rare Dis
Sivadasan A, Hernandez A, Candido E, Parkin PC, Tu K, Mendoza M, Barnett-Tapia C.   +6 more
europepmc   +1 more source

An Isolated Case of Unilateral Macro-Ophthalmia With Resultant Anisometropic Amblyopia in Neurofibromatosis 1. [PDF]

Cureus, 2023
Mukit FA, Cape HT, Huq SS, Bohn S.
europepmc   +1 more source

Supplementary Material for: Highly Active Relapsing-Remitting Multiple Sclerosis (RRMS) with Neurofibromatosis Type 1 (NF1). Radiological aspects and therapeutic challenges - Case report

M. Lemonaris, Kleopa K.A.
openalex   +1 more source

Mediastinal mass in an tuberculosis-exposed 2-year old child with neurofibromatosis type 1 – TB or not TB?

, 2020
Renate Krüger, Cornelia Potratz, Pablo Hernáiz Driever, Birgit Lala, Cornelia Feiterna‐Sperling   +4 more
openalex   +2 more sources

Malignant peripheral nerve sheath tumours in neurofibromatosis 1

Journal of Medical Genetics, 2002
D. Evans, M. Baser, J. McGaughran, S. Sharif, E. Howard, A. Moran   +5 more
semanticscholar   +1 more source

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
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