Results 221 to 230 of about 108,120,995 (240)

[From gene to disease; neurofibromatosis type 1].

Nederlands tijdschrift voor geneeskunde, 2001
Neurofibromatosis type 1 (NF1) is an autosomal dominant disease characterised by café-au-lait spots, freckling in the axillary or inguinal region, dermal and plexiform neurofibromas and Lisch nodules. Complications are severe in one third of patients, and the clinical variability is pronounced, even within families.
A, de Goede-Bolder, M H, Cnossen, D, Dooijes, A M, van den Ouweland, M F, Niermeijer   +4 more
openaire   +1 more source

Management of neurofibromatosis type 1-associated plexiform neurofibromas

Neuro-Oncology, 2022
Kaleb Yohay, Robert Listernick, Nicole J Ullrich   +2 more
exaly  

Histogenesis control genes and neurofibromatosis 1

European Journal of Pediatrics, 2000
openaire   +1 more source

Neurofibromatosis type 1 and chronic neurological conditions in the United States: an administrative claims analysis

Genetics in Medicine, 2015
Margaret A Olsen, David H. Gutmann, Kimberly J Johnson   +2 more
exaly  

Neurofibromatosis type 1 gene

1993
WHITE RAYMOND L, O'CONNELL PETER, VISKOCHIL DAVID H, CAWTHON RICHARD M   +3 more
openaire   +1 more source

Consortium Closing in on Neurofibromatosis Type 1 Gene

JNCI Journal of the National Cancer Institute, 1989
openaire   +1 more source

Massive Subperiosteal Hemorrhage in Neurofibromatosis

Radiology, 1977
Issa Yaghmai
exaly  

Wilms' tumor and neurofibromatosis

Ca-A Cancer Journal for Clinicians, 1982
exaly  

The different forms of neurofibromatosis

Child's Nervous System, 1999
Martino Ruggieri
exaly  

Plexiform Neurofibromas in Children with Neurofibromatosis Type 1: Frequency and Associated Clinical Deficits

Journal of Pediatrics, 2011
Rosa Nguyen, Lan Kluwe, Victor-Felix Mautner   +2 more
exaly