Results 111 to 120 of about 1,927 (190)

Ovarian cell tumor in a child with neurofibromatosis type 1.

Ann Afr Med, 2022
Qutub LM, Al-Agha AE.
europepmc   +1 more source

Molekularbiologie in der Neurologie [PDF]

, 1994
Borasio, Gian Domenico, Brandt, T., Gasser, T.   +2 more
core  

Leber´s hereditary optic neuroretinopathy [PDF]

, 1993
Janetzky, B., Klopstock, Thomas, Lindner, A., Reichmann, Heinz, Schneider, C., Seibel, P., Toyka, K., Trappe, J.   +7 more
core   +1 more source

Whole-body MRI-based long-term evaluation of pediatric NF1 patients without initial tumor burden with evidence of newly developed peripheral nerve sheath tumors. [PDF]

Orphanet J Rare Dis
Schmalhofer ML, Farschtschi S, Kluwe L, Mautner VF, Adam G, Well L, Ristow I.   +6 more
europepmc   +1 more source

Altered structural networks and cognitive functioning in long-term survivors of pediatric brain tumors. [PDF]

Neuroimage Rep
Bullens K, Sleurs C, Blommaert J, Gavrila Laic RA, Radwan A, De Roeck L, Dupont P, Lemiere J, Jacobs S.   +8 more
europepmc   +1 more source

Hétérochromie irienne causée par le syndrome de Waardenburg chez un nourrisson de 2 mois. [PDF]

CMAJ
Lin PA, Hung JH, Huang YH.
europepmc   +1 more source

Troubles de la communication chez les enfants atteints de neurofibromatose de type 1

Glossa, 1996
Cynthia Solot, Elaine Zackai, Angela Obringer, Dan Konkle, Steven Handler, Anna Meadows   +5 more
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  

Atypical Multifocal Granular Cell Tumor with FLT3 Y842C Somatic Mutation: A case report and a review of the literature. [PDF]

Tunis Med
Zara Rozalen A, Garcia R, Husami S, Marino G, Nava VE.   +4 more
europepmc   +1 more source

Experiences of stigmatization and its impacts among individuals living with hereditary diseases and family members in Portugal: an exploratory study. [PDF]

J Community Genet
Valentim J, Paneque M, Mendes Á.
europepmc   +1 more source