Results 81 to 90 of about 1,890 (196)

Hypertrichose [PDF]

, 2018
Zusammenfassung: Hypertrichose bezeichnet, auf Lokalisation, Alter, Geschlecht und ethnische Provenienz bezogen, übermäßiges, diffuses oder umschriebenes Haarwachstum, das nicht dem Verteilungsmuster der sekundären männlichen Geschlechtsbehaarung ...
Trüeb, R.M.
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Tumor maligno da bainha dos nervos periféricos do pulmão: A propósito de um caso clínico Malignant peripheral nerve sheath tumors: A case report

Revista Portuguesa de Pneumologia, 2010
Os tumores malignos da bainha dos nervos periféricos correspondem a um grupo raro de sarcomas de tecidos moles que tendem a ocorrer em doentes com neurofibromatose tipo 1 ou vários anos após tratamentos de radioterapia.
N Serrano Marçal, E Teixeira, R Sotto-Mayor, A Manique, P Campos, J Cruz, M Mendes de Almeida, A Bugalho de Almeida   +7 more
doaj  

vGanglioneurome médiastianal au cours de la neurofibromatose de Von Recklinghausen [Mediastinal ganglioneuroma in the neurofibromatosis of Von Recklinghausen]

Journal de la Faculté de Médecine d'Oran
Résumé Introduction - La neurofibromatose de Von Recklinghausen (NF1) est une maladie à transmission autosomique dominante, son incidence est estimée à 1/3000 naissances.
Malika Metahri, Abdelmadjid Snouber, Samir Bensaifi, Souad Maaroufi   +3 more
doaj  

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

Portuguese study of familial dilated cardiomyopathy: the FATIMA study [PDF]

, 2008
Dilated cardiomyopathy (DCM) is a myocardial disease, characterized by ventricular dilatation and impaired systolic function, that in more than 30% of cases has a familial or genetic origin. Given its age-dependent penetrance, DCM frequently manifests in
Abreu-Lima, C., Bicho, M., Bourbon, M., Brito, D., Ceia, F., Correia, M.J., Fonseca, C., Madeira, H., Martins, E., Moura, B., Perdigão, C., Rebocho, M.J., Silva-Cardoso, J.   +12 more
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Anatomy Teaching at the School of Health Sciences of University of Minho [PDF]

, 2016
info:eu-repo/semantics ...
Almeida, António Manuel Melo Soares, Amorim, João Filipe Pinheiro, Braga, Isaac, Cerqueira, João José, Lamas, Nuno Jorge, Martins, Sandra, Mendes, Sofia Silva, Miguelote, Rui Filipe Oliveira, Morgado, Pedro, Oliveira, Tiago Gil, Peixoto, João Miguel Seiça Bessa, Pereira, Vitor H., Sousa, Nuno, Teixeira, Pedro Alexandre Leão Araújo Gonçalves   +13 more
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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

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
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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