Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Mariam Patrícia Auada"'
Autor:
José Thiago de Souza de Castro, Camilo Lotfi Saab, Mariam Patrícia Auada Souto, Juliane Giselle Ortolam, Carlos Eduardo Steiner, Thiago Junqueira Ribeiro de Rezende, Fabiano Reis
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 81, Iss 09, Pp 809-815 (2023)
Background Sjogren-Larsson syndrome (SLS) is a neurocutaneous disease with an autosomal recessive inheritance, caused by mutations in the gene that encodes fatty aldehyde dehydrogenase (ALDH3A2), clinically characterized by ichthyosis, spastic dipleg
Externí odkaz:
https://doaj.org/article/f3ca6498b01547468c055233a214e434
Akademický článek
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Autor:
Castro, José Thiago de Souza de, Saab, Camilo Lotfi, Souto, Mariam Patrícia Auada, Ortolam, Juliane Giselle, Steiner, Carlos Eduardo, Rezende, Thiago Junqueira Ribeiro de, Reis, Fabiano
Publikováno v:
Arquivos de Neuro-Psiquiatria; September 2023, Vol. 81 Issue: 9 p809-815, 7p
Publikováno v:
Aesthetic plastic surgery. 45(5)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::edf10c09d1d38c5966df22b11d89369f
https://pubmed.ncbi.nlm.nih.gov/33881605
https://pubmed.ncbi.nlm.nih.gov/33881605
Publikováno v:
Journal of cosmetic dermatologyREFERENCES. 20(5)
Background In the lower third of the face, botulinum toxin A is used to obtain a more harmonious contour. The anatomical complexity of the face requires a more precise application of botulinum toxin. Aim Describe the treatment of an unexpected effect
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cb533d46644cfa0cc9961696f2a51a6e
https://pubmed.ncbi.nlm.nih.gov/33249739
https://pubmed.ncbi.nlm.nih.gov/33249739
Akademický článek
Tento výsledek nelze pro nepřihlášené uživatele zobrazit.
K zobrazení výsledku je třeba se přihlásit.
K zobrazení výsledku je třeba se přihlásit.
Autor:
Edi Lúcia Sartorato, Fabiana Alexandrino, William B Rizzo, Maria Letícia Cintra, G. Carney, T. S. Aguiar, C. E. Steiner, R. D. Azulay, Mariam Patrícia Auada, Maria Beatriz Puzzi
Publikováno v:
British Journal of Dermatology. 154:770-773
Sjogren–Larsson syndrome (SLS; OMIM 270200) is an autosomal recessive disorder characterized by the presence of pruritic ichthyosis, mental retardation, spastic diplegia or tetraplegia, retinal perimacular ‘glistening white dots’ and photophobi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4fc4275f0ce3f22e52873bdab072ad18
https://doi.org/10.1111/j.1365-2133.2006.07135.x
https://doi.org/10.1111/j.1365-2133.2006.07135.x
Autor:
Marcus de Medeiros Matsushita, Graziela de Macedo Matsushita, Mariam Patrícia Auada Souto, Luís Ricardo Martinhão Souto
Publikováno v:
Journal of Dermatological Case Reports. 7
Background Pilomatrixoma (OMIM ID #132600) is a benign cutaneous tumor originating from the pilosebaceous follicle and characterized by the presence of subcutaneous nodules of up to 3.0 cm in diameter, usually on the head, neck and upper extremities.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::709f6e8cfb22029981a02cb20fda43a5
https://doi.org/10.3315/jdcr.2013.1141
https://doi.org/10.3315/jdcr.2013.1141
Autor:
Maria Beatriz Puzzi, Mariam Patrícia Auada, Denise Pontes Cavalcanti, Danilo Viana, Maria Letícia Cintra
Publikováno v:
Clinical dysmorphology. 13(3)
Lymphoedema and skin naevi are common in children with Turner syndrome (TS). Lymphoedema in the early stages of fetal life is thought to cause several of the phenotypic characteristics in patients with TS such as nuchal folds and pterygium colli. We
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bba9e42a49eabb2ec20e6bde85f420c
https://pubmed.ncbi.nlm.nih.gov/15194953
https://pubmed.ncbi.nlm.nih.gov/15194953
Autor:
Mariam Patrícia, Auada, Maria Beatriz Puzzi, Taube, Edgard F, Collares, Ana Maria Uthida, Tanaka, Maria Letícia, Cintra
Publikováno v:
European journal of dermatology : EJD. 12(3)
Sjögren-Larsson syndrome is a rare disorder that consists of congenital ichthyosis and neurological symptoms due to an enzymatic defect of fatty aldehyde dehydrogenase in the fatty alcohol cycle. We report three cases of Sjögren-Larsson syndrome in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::c4930cae2a439d202588b32e59b6b54f
https://pubmed.ncbi.nlm.nih.gov/11978568
https://pubmed.ncbi.nlm.nih.gov/11978568