Results 191 to 200 of about 34,784,083 (239)

Circulating Tumor DNA in Neurofibromatosis Type 1: Translating Molecular Discovery into Clinical Surveillance. [PDF]

Diagnostics (Basel)
Vargas JV, Tosello V, Pigato G, Indraccolo S, Chiara F.   +4 more
europepmc   +1 more source

Coexistence of Endodermal Cyst and Neurofibromatosis Type 1: A Case Report. [PDF]

Cureus
Takano K, Inoue Y, Oi Y, Kawajiri T, Hohri T.   +4 more
europepmc   +1 more source

Everyday executive functions in children with neurofibromatosis type 1: Data from nine institutions. [PDF]

Neuropsychology
Zong X, Liu D, Wu X, Wolters PL, Payne JM, Klein-Tasman BP, Walsh KS, Janusz J, Pride N, Morris SM, Bearden CE, Stavinoha PL, Hou Y.   +12 more
europepmc   +1 more source

Rare Association Between Neurofibromatosis Type 1 and Adrenocortical Carcinoma. [PDF]

Clin Case Rep
Pluim Z, Choi JDW, Kakala B, Wong J, Clifton-Bligh R, Sywak M, Howle J.   +6 more
europepmc   +1 more source

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Von Recklinghausen's neurofibromatosis: neurofibromatosis type 1

Lancet, The, 2003
Rebecca M Reynolds, I W Campbell
exaly   +3 more sources

Neurofibromatosis type 1

Biochimica et Biophysica Acta (BBA) - Reviews on Cancer, 2000
Neurofibromatosis 1 (NF1) is an autosomal dominant neurocutaneous disorder with an incidence of approximately 1 in 4000. Cognitive deficits and academic learning difficulties are the most common neurological 'complication' of NF1 in childhood and can be responsible for significant lifetime morbidity.
openaire   +4 more sources

Neurofibromatosis type 1 and pregnancy

American Journal of Medical Genetics, 1996
Neurofibromatosis Type 1 (NF-1) is an autosomal dominant condition which has markedly variable clinical expression, with manifestations ranging from mild cutaneous lesions to severe orthopedic complications and functional impairment. The current obstetrical literature indicates that women with NF-1 have increased complications associated with pregnancy.
L, Dugoff, E, Sujansky
openaire   +2 more sources

Pathophysiology of Neurofibromatosis Type 1

Annals of Internal Medicine, 2006
Neurofibromatoses are inherited disorders, designated as neurofibromatosis type 1 (NF1), neurofibromatosis type 2, and schwannomatosis, that tend to result in benign tumors of the nerve sheath.
Amy, Theos, Bruce R, Korf
openaire   +2 more sources

Neurofibromatosis type 1

2015
Neurofibromatosis type 1 (NF1), previously known as von Recklinghausen disease, is a neurogenetic disorder distinct from neurofibromatosis type 2 (NF2). Approximately 1:2500 to 1:3500 individuals worldwide are affected, regardless of ethnicity or race.
Jacqueline L, Anderson, David H, Gutmann
openaire   +2 more sources