Results 91 to 100 of about 1,927 (190)

[An unusual cause of tarsal tunnel syndrome in a 15-year-old girl: about a case]. [PDF]

Pan Afr Med J, 2022
Abdelkrim EH, Douma H, Barchah O, Elkasseh M, Boumaiz A, Belkyal S, Haoury HE, Madhar M, Chafik R, Najeb Y.   +9 more
europepmc   +1 more source

Toward an Early Diagnosis for Alzheimer's Disease Based on the Perinuclear Localization of the ATM Protein. [PDF]

Cells, 2023
Berthel E, Pujo-Menjouet L, Le Reun E, Sonzogni L, Al-Choboq J, Chekroun A, Granzotto A, Devic C, Ferlazzo ML, Pereira S, Bourguignon M, Foray N.   +11 more
europepmc   +1 more source

Manifestations buccales de la neurofibromatose de type 1

, 2017
La neurofibromatose de type 1 appelée maladie de Von Recklinghausen ou NF1 est une maladie multi- viscérale d’origine génétique de sévérité très variable. Elle se manifeste par des taches brunes de type « café au lait » sur la peau et par des neurofibromes : des tumeurs situées le long des nerfs.
openaire   +1 more source

Unexpected Small-Bowel Finding in Overt-Obscure Gastrointestinal Bleeding in a Patient with Neurofibromatosis Type 1 and Crohn's Disease. [PDF]

GE Port J Gastroenterol, 2022
Gomes C, Ponte A, Pinho R, Rodrigues A, Carvalho J.   +4 more
europepmc   +1 more source

[OCULO-ORBITAL TUMOURS AT THE NATIONAL UNIVERSITY HOSPITAL CENTRE OF BANGUI (CNHUB), CENTRAL AFRICAN REPUBLIC, IN 2022]. [PDF]

Med Trop Sante Int, 2023
Elien Gagnan Yan Zaou Tou RR, Mbaïkoua JM, Kosh Komba Palet JE, Guirou N.   +3 more
europepmc   +1 more source

Neurofibromatosis : evaluation of the epidemiological profile of patients and the impact of the disease on government programs for the Integrated Development Region of the Federal District and surrounding areas (RIDE-DF) in 2013 [PDF]

, 2015
Monografia (graduação)—Universidade de Brasília, Faculdade de Ciências da Saúde, Departamento de Saúde Coletiva, 2015.A neurofibromatose (NF) é uma doença rara, decorrente de uma desordem de causa genética autossômica dominante, caracterizando duas ...
Amorim, Marcos Antonio de
core  

Neurofibromatosis type 1. [PDF]

Radiol Bras, 2022
Mançano AD.
europepmc   +1 more source

[Long-Term Pulmonary Function after Combined Anteroposterior Spinal Fusion for Scoliosis in Neurofibromatosis Type 1 and Marfan Syndrome at a Mean Follow-Up of 13 Years]. [PDF]

Rev Bras Ortop (Sao Paulo)
Oliveira JAA, Visconti RDR, Azevedo GBL, Barros AGC, Carelli LE, Silva JRLE.   +5 more
europepmc   +2 more sources

[McCune-Albright syndrome: a case report and literature review]. [PDF]

Pan Afr Med J, 2023
Chabouni H, Jemaa MB, Ghorbel M, Trigui M, Zribi W, Zribi M, Ayadi K, Aoui M, Keskes H.   +8 more
europepmc   +1 more source

Steady-state visual evoked potentials in children with neurofibromatosis type 1: associations with behavioral rating scales and impact of psychostimulant medication. [PDF]

J Neurodev Disord, 2022
Lalancette E, Charlebois-Poirier AR, Agbogba K, Knoth IS, Jones EJH, Mason L, Perreault S, Lippé S.   +7 more
europepmc   +1 more source