Výsledky vyhledávání - "E T, Pereira"

Do Gender Quotas Lead to Gender Equality?

Autor: E. T. Pereira, L. Marinò, S. Salaris

Publikováno v: Gender Studies, Entrepreneurship and Human Capital ISBN: 9783030468736

The number of women in the boards of directors has increased in a lot of international firms, in recent years, with the help of the gender quotas, but we do not know whether this fact leads to an increase in gender equality. Based on a literature rev

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9437d5209542e92ead60e4cdfb24b1d6
https://doi.org/10.1007/978-3-030-46874-3_10

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Huntington disease and Huntington disease-like in a case series from Brazil

Publikováno v: Clinical genetics. 86(4)

The aim of this study was to identify the relative frequency of Huntington's disease (HD) and HD-like (HDL) disorders HDL1, HDL2, spinocerebellar ataxia type 2 (SCA2), SCA17, dentatorubral-pallidoluysian degeneration (DRPLA), benign hereditary chorea

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::98dfb317b50f7639a197db4c44f21da0
https://pubmed.ncbi.nlm.nih.gov/24102565

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Prenatal diagnosis of bilateral proximal femoral hypoplasia

Autor: G. R. De Luca, D. A. Vitorello, L. F. Gonçalves, E. T. Pereira, H. Philippi, L. M. M. Parente, J. A. Saab Neto

Publikováno v: Ultrasound in Obstetrics and Gynecology. 8:127-130

Proximal femoral focal deficiency is a rare skeletal disorder, with an estimated incidence of 0.11 to 0.2/10 000 births. The bilateral form is uncommon, occurring in 10 to 15% of cases. We report a case of bilateral proximal femoral focal deficiency

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::a3bf4d0529538b5b7cc50fe3b1a5d03b
https://doi.org/10.1046/j.1469-0705.1996.08020127.x

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Cutaneous hemangioma of the thigh: prenatal diagnosis

Autor: U. C. Barbosa, L. F. Gonçalves, J. Abi Saab Neto, L. M. M. Parente, E. T. Pereira, D. A. Vitorello

Publikováno v: Ultrasound in Obstetrics and Gynecology. 9:128-130

We report a case of cutaneous hemangioma of the thigh detected by prenatal ultrasound. A hypoechoic homogeneous mass, filled with low-density echoes, was visualized on the posterior aspect of the right thigh, close to the genital region, at 36 weeks.

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::fe848c3a7d800ce991c84c78633f276e
https://doi.org/10.1046/j.1469-0705.1997.09020128.x

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Klippel-Trenaunay-Weber syndrome presenting as massive lymphangiohemangioma of the thigh: prenatal diagnosis

Autor: L F, Gonçalves, M V, Rojas, D, Vitorello, E T, Pereira, M, Pereima, J A, Saab Neto

Publikováno v: Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 15(6)

We report a case of Klippel-Trenaunay-Weber syndrome presenting prenatally as a massive congenital lymphangiohemangioma of the thigh. Routine ultrasonographic examination revealed multiple distorted cystic areas extending from the right flank through

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::dff4638f9efe304b44d386fa334d6346
https://pubmed.ncbi.nlm.nih.gov/11005126

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Cutaneous hemangioma of the thigh: prenatal diagnosis

Autor: L F, Gonçalves, E T, Pereira, L M, Parente, D A, Vitorello, U C, Barbosa, J A, Saab Neto

Publikováno v: Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 9(2)

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::33f63338513643e618b22da930dda98a
https://pubmed.ncbi.nlm.nih.gov/9132256

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Prenatal diagnosis of bilateral proximal femoral hypoplasia

Autor: L F, Gonçalves, G R, De Luca, D A, Vitorello, L M, Parente, H, Philippi, J A, Saab Neto, E T, Pereira

Publikováno v: Ultrasound in obstetricsgynecology : the official journal of the International Society of Ultrasound in Obstetrics and Gynecology. 8(2)

Proximal femoral focal deficiency is a rare skeletal disorder, with an estimated incidence of 0.11 to 0.2/10,000 births. The bilateral form is uncommon, occurring in 10 to 15% of cases. We report a case of bilateral proximal femoral focal deficiency

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::5c4ae4b6914e14113984f79f66afd1af
https://pubmed.ncbi.nlm.nih.gov/8883317

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'Pure' partial trisomy 3p due to the malsegregation of a balanced maternal translocation t (X;3) (p22.3;p21)

Autor: J C, de Almeida, D F, Reis, J C, Llerena, E T, Pereira

Publikováno v: Annales de genetique. 32(3)

The authors present the clinical and cytogenetic studies of a white malformed baby with dup (3p) secondary to the malsegregation of a maternal balanced (X;3) (p22.3;p21) translocation. Besides the typical clinical features he also presented polydacty

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::1fbc0b9475a4a9472e03f60e6ce65610
https://pubmed.ncbi.nlm.nih.gov/2817779

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Ring 13 in an adult male with a 13:13 translocation mother

Autor: J C, de Almeida, J C, Llerena, D M, Gomes, R R, Martins, E T, Pereira

Publikováno v: Annales de genetique. 26(2)

A male with a ring 13 chromosome [r(13)(p11q34)], mild mental retardation, short stature, oligoasthenospermia, and few dysmorphisms is reported. His mother who had a poor reproductive history is carrier of a t(13q13q), featuring a dicentric NOR-negat

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=pmid________::d70d739ea64e55014fc371204272f48c
https://pubmed.ncbi.nlm.nih.gov/6604485

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