Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Osvaldo Mutchinick"'
Autor:
Felipe Vilchis, Bertha Chávez, Gregorio Pérez-Palacios, Patricia Canto, Alfredo Ulloa-Aguirre, Juan Pablo Méndez, Julianne Imperato-McGinley, Osvaldo Mutchinick
Publikováno v:
Clinical Endocrinology. 46:155-160
Background and objective Male pseudohermaphroditism due to 5 alpha-reductase deficiency was originally described in 1974. Recently, 5 alpha-reductase Type 2 gene defects have been found generally to be due to point mutations within the 5 exons of the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::828b4bfef1bfa92f5c758f8baa7a8dd1
https://doi.org/10.1046/j.1365-2265.1997.800904.x
https://doi.org/10.1046/j.1365-2265.1997.800904.x
Publikováno v:
Journal of the American College of Cardiology. 27:1698-1703
Objectives. This report describes our experience with the use of an anticoagulant regimen of adjusted doses of subcutaneous heparin during pregnancy in women with cardiac valve prostheses. Background. Gravid patients with prosthetic heart valves requ
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eab46d7b5611f77234580ddf87913eb6
https://doi.org/10.1016/0735-1097(96)00072-1
https://doi.org/10.1016/0735-1097(96)00072-1
Autor:
Neal A. Musto, Osvaldo Mutchinick, Fernando Larrea, Julio Granados, Vicente Díaz-Sánchez, Rosa Maria Oliart
Publikováno v:
Journal of Steroid Biochemistry. 36:541-548
Human sex hormone-binding globulin (hSHBG) is a plasma glycoprotein composed of two identical subunits. The protein, which has high affinity for testosterone and estradiol has been purified to homogeneity. In this study we have investigated, on neura
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::87121f769424627863a0a7372514ad92
https://doi.org/10.1016/0022-4731(90)90171-n
https://doi.org/10.1016/0022-4731(90)90171-n
Autor:
Hester Y, Kroes, Richard S, Olney, Aldo, Rosano, Yecai, Liu, Eduardo E, Castilla, Guido, Cocchi, Catherine, De Vigan, María L, Martínez-Frías, Pierpaolo, Mastroiacovo, Paul, Merlob, Osvaldo, Mutchinick, Annukka, Ritvanen, Claude, Stoll, Anthonie J, van Essen, Jan Maarten, Cobben, Martina C, Cornel
Publikováno v:
American journal of medical genetics. Part A. (2)
Dieker and Opitz in 1969 described the simultaneous occurrence of limb deficiencies (LDs) and renal anomalies (RAs) in three patients. Curran and Curran introduced in 1972 the term "acrorenal syndrome." Since then, the term "acrorenal syndrome" is us
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::b7ad6085b76d85c473d4ae497239b8e4
https://pubmed.ncbi.nlm.nih.gov/15316969
https://pubmed.ncbi.nlm.nih.gov/15316969
Autor:
Rubén Lisker, Ricardo Correa-Rotter, Sergio Sanchez, Osvaldo Mutchinick, Sergio Ponce de Leon Rosales, Salomón Jasqui, María Aranda López
Publikováno v:
Scopus-Elsevier
1 * Abstract It has been reported that Vitamin D receptor polymorphisms are associated with osteoporosis, particularly those demonstrated by the BsmI and Fok I restriction enzymes. Herein we report the results of a case-control study performed in pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::accf7ecb409c40a7eaffcee46cb3cb0b
https://pubmed.ncbi.nlm.nih.gov/14527203
https://pubmed.ncbi.nlm.nih.gov/14527203
Autor:
Alfredo Ulloa-Aguirre, Osvaldo Mutchinick, Susana Kofman-Alfaro, Gregorio Pérez-Palacios, Carlos Fernández-del-Castillo, Juan Pablo Méndez, Edgardo Reyes
Publikováno v:
Obstetrical & Gynecological Survey. 48:756-758
We describe clinical, cytogenetic, endocrine, and histopathological findings in 16 patients with mixed gonadal dysgenesis (MGD). All patients except 1 presented genital ambiguity and 10 of them had Ullrich-Turner manifestations. The 45,X/46,XY karyot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3d38d364b818bc2db53385b310947d56
https://doi.org/10.1097/00006254-199311000-00021
https://doi.org/10.1097/00006254-199311000-00021
Autor:
Renata Rivera, Cesar Vargas-Serafin, Guadalupe Jiménez, Olga Barrales, Georgina Barrera, Osvaldo Mutchinick, Christianne Bourlon, Deborah Martínez-Baños, Virginia Santiago-Cano
Publikováno v:
Blood. 124:5709-5709
Background Multiple myeloma (MM) has been associated with several cytogenetic abnormalities (CA), contributing in heterogeneity of clinical outcome. CA are not always captured by conventional cytogenetic analysis (CGA), fluorescence in situ hybridiza
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a23bf5bb9289aab16b63112886d438ec
https://doi.org/10.1182/blood.v124.21.5709.5709
https://doi.org/10.1182/blood.v124.21.5709.5709
Autor:
Osvaldo Mutchinick, María E. Gonsebatt
Publikováno v:
Mutation research. 243(4)
Human lymphocyte proliferation kinetics was studied in different culture conditions including synthetic medium, Hanks' BSS and Hanks' supplemented with autologous plasma at several culture times. Even though mitotic indices (MI) were low, lymhocytes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e0685589bdf452cc9574059cd2a5cbb7
https://pubmed.ncbi.nlm.nih.gov/2325691
https://pubmed.ncbi.nlm.nih.gov/2325691
Autor:
Gregorio Pérez-Palacios, Osvaldo Mutchinick, Nereo Escobar, Martha Medina, Susana Kofman, Rubén Lisker, Lizbeth Ruz, Mario García
Publikováno v:
Human Genetics. 58:373-376
Cytogenetic and endocrine studies were performed in five unrelated 45,X/46,XY individuals in an attempt to correlate them with their clinical expression and gonadal morphology. A lack of a consistent pattern between cytogenetic findings and phenotype
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a7d702f266120dcbfbaabb540fff623
https://doi.org/10.1007/bf00282818
https://doi.org/10.1007/bf00282818
Autor:
Rubén Lisker, Andrés Hernández, Manuel Martínez-Lavin, Osvaldo Mutchinick, Cristina Armas, Pedro Reyes, Javier Robles-Gil, John M. Optiz
Publikováno v:
American Journal of Medical Genetics. 3:389-395
Gerodermia osteodysplastica hereditaria was diagnosed in three Mexican brothers 6, 7, and 8 years old, respectively, who had the distinct facial appearance with sagging cheeks, premature wrinkling of the skin of face, abdomen, and dorsum of hands and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::191234f6d481d3cfa84835dd31509373
https://doi.org/10.1002/ajmg.1320030410
https://doi.org/10.1002/ajmg.1320030410