Results 101 to 110 of about 1,890 (196)

Neurofibromin expression by normal salivary glands. [PDF]

Head Face Med, 2021
Luna EB, Montovani PP, Rozza-de-Menezes RE, Cunha KS.   +3 more
europepmc   +1 more source

Endocrine and non-endocrine causes of fatigue in adults with Neurofibromatosis type 1. [PDF]

Front Endocrinol (Lausanne), 2023
Rosenberg AGW, Mochèl K, Hähner LM, Ruules L, Davidse K, Bos-Roubos AG, van Dijk SA, Zillikens MC, Taal W, van der Lely AJ, de Graaff LCG.   +10 more
europepmc   +1 more source

Hypertrophie gingivale mandibulaire révélatrice d’une neurofibromatose de type 1 [PDF]

62ème Congrès de la SFCO, 2014
MP Pédeboscq, S Catros, JC Fricain
openaire   +1 more source

Évaluation des corrélations phénotype-génotype dans la neurofibromatose de type 1

, 2016
La neurofibromatose de type 1 (NF1 ; numéro OMIM 162200), ou maladie de Von Recklinghausen, est l'une des maladies génétiques rares les plus fréquentes. Elle a une répartition mondiale homogène et une incidence estimée à 1 cas pour 2500 naissances. Il s'agit d'une maladie à transmission autosomique dominante dont la pénétrance est quasi-complète à l ...
da Silva, Alexandre, Metaane, Selma, Pizzighella, Sandro, Curis, Emmanuel, Sabbagh, Audrey, Nicolis, Ioannis   +5 more
openaire   +1 more source

[Von Recklinghausen's disease revealed by a thoracic mass and pulmonary cystic lesions]. [PDF]

Pan Afr Med J
Laatfa I, Lachraf H.
europepmc   +1 more source

L'évaluation, le diagnostic et la prise en charge du trouble développemental de la coordination. [PDF]

Paediatr Child Health, 2021
Ip A, Mickelson ECR, Zwicker JG.
europepmc   +1 more source

Neurofibromatosis type 1 and phaeochromocytoma: a clinical case report [PDF]

, 2011
Alves, P, Barbosa, B, Batista, M, Fonseca, I, Norte, A, Saldanha, MH   +5 more
core  

Toward Understanding the Mechanisms of Malignant Peripheral Nerve Sheath Tumor Development. [PDF]

Int J Mol Sci, 2021
Mohamad T, Plante C, Brosseau JP.
europepmc   +1 more source

Proposta de modificação dos critérios diagnósticos para neurofibromatose tipo 1 [PDF]

Of the patients with Legius syndrome, 2 % completes the diagnostic approaches of neurofibromatosis type since 1 they present brown stain with milk and sign of Crowe, this makes indistinguishable the two diseases.
Feria Rosales, Orendys, López Toranzo, Yasaris, Rodríguez Carbonell, Lisdany, Rodríguez Torres, Teresa Petra, Velázquez Avila, Yordania   +4 more
core   +1 more source

Neurofibromatosis type 1: evaluation by chest computed tomography. [PDF]

Radiol Bras, 2021
Alves Júnior SF, Irion KL, de Melo ASA, Meirelles GSP, Rodrigues RS, Souza AS, Hochhegger B, Zanetti G, Marchiori E.   +8 more
europepmc   +1 more source