Results 81 to 90 of about 510 (170)

Nodules de lisch dans la maladie de Von Recklinghausen

PAMJ Clinical Medicine, 2019
La maladie de Von Recklinghausen est une maladie systémique génétique et hétérogène. L´atteinte oculaire au cous de cette phacomatose est rare mais pathognomonique.
Kawtar Hessaki
doaj   +1 more source

Ressecção do tumor e colocação de enxerto de pele parcial no couro cabeludo em um paciente com neurofibromatose tipo 1

Revista Brasileira de Cirurgia Plástica
A neurofibromatose tipo 1 (NF1) é um distúrbio neurocutâneo hereditário no qual se formam tumores no sistema nervoso (neurofibromas). Os neurofibromas são os tumores benignos mais comuns na NF1.
ELIZBET SUSAN MONTES-MADARIAGA, BRANDO ORTIZ-SAAVEDRA, EULER ALTAMIRANO-FARFAN, JIMMY PUMAMANGO-CORDOVA, MELISSA HERENCIA-ANAYA   +4 more
doaj   +1 more source

[Cosmetic and functional results after resection of cutaneous neurofibroma in neurofibromatosis type 1 : Operation of neurofibroma improves quality of life while having moderate complications]. [PDF]

Dermatologie (Heidelb), 2022
Walz B, Pfefferle V, Häfner HM, Kofler L.   +3 more
europepmc   +1 more source

[Clinical aspects of Neurofibromatosis type 1 seen in the Department of Dermatology at University Hospital Antananarivo, Madagascar]. [PDF]

Med Trop Sante Int, 2022
Sendrasoa FA, Rasoarisata A, Ramarozatovo LS, Rapelanoro Rabenja F.   +3 more
europepmc   +1 more source

Neurofibromatosis type 1, fibromuscular dysplasia, and ischemic stroke: an association lost in time? A case report. [PDF]

J Vasc Bras, 2023
da Fonseca IO, Luvizutto GJ, Souza IP, Trindade AP, de Freitas CCM, Bazan R, Modolo GP.   +6 more
europepmc   +1 more source

[Lisch nodules: an ophthalmic marker of neurofibromatosis type 1]. [PDF]

Pan Afr Med J, 2022
Bouirig K, Cherkaoui LO.
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

MULTIPLE NEUROENDOCRINE NEOPLASIA IN A PATIENT WITH TYPE I NEUROFIBROMATOSIS (NF1): REPORT OF A NEW MUTATION (NF1, EXONS 2-30 DELETION) AND LITERATURE REVIEW. [PDF]

Arq Bras Cir Dig, 2023
Kanno DT, Mattos RLM, Campos FG, Siqueira RM, Carvalho RB, Real Martinez CA.   +5 more
europepmc   +1 more source

[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