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Premature ovarian insufficiency: A review [Insuficiencia ov�rica prematura: una revisi�n]
(2012)
Premature ovarian insufficiency is characterized by primary or secondary amenorrhea, hypoestrogenism and elevated levels of FSH (follicle stimulating hormone), which affects 1 in 100 women under 40 years. Its etiology is ...
Further clinical delineation in trisomy 1q32 syndrome
(2001)
A male newborn with multiple congenital abnormalities was studied. Clinically, he showed prominent forehead, facial dysmorphism, ear malformations, congenital heart defect and limb anomalies. The cytogenetic studies ...
Homocysteine, MTHFR C677T and A1298C polymorphisms, and clinical and biochemical variables in the mexican population [Homociste�na, polimorfismos MTHFR C677T, A1298C e vari�veis cl�nico-bioqu�micas em popula��o mexicana]
(2014)
The objective of the current work was to analyze the relationship of serum homocysteine (Hcy) with MTHFR C677T and A1298C polymorphisms and clinical and biochemical variables in the Mexican population. Hcy (immunoassay) ...
Iron binding to nutrients containing fiber and phenytoin
(1986)
1. 1. Ascorbate and citrate extracted more iron than EDTA from pig foodstuffs (P < 0.001). 2. 2. Glucose-saline solution (GSS) and ascorbate were less capable than citrate of extracting iron from maize tortilla (P < 0.001). ...
Paternal isodisomy 7q secondary to monosomy 7 at recurrence in a Down syndrome child with acute myelogenous leukemia
(2002)
We report a boy with Down syndrome and leukemia who acquired uniparental isodisomy of chromosome 7q as a secondary chromosomal change during recurrence of the disease. His karyotype before therapy was 46,XY,der(1)t(1;1)( ...
Sensitization of cervix cancer cells to Adriamycin by Pentoxifylline induces an increase in apoptosis and decrease senescence
(2010)
Background: Chemotherapeutic drugs like Adriamycin (ADR) induces apoptosis or senescence in cancer cells but these cells often develop resistance and generate responses of short duration or complete failure. The methylxantine ...
Ophthalmic manifestations in Mexican patients with Fabry disease [Manifestaciones oftalmol�gicas en pacientes mexicanos con enfermedad de Fabry]
(2012)
Fabry disease (FD) is a rare X-linked genetic lysosomal storage disease caused by a deficiency of the enzyme ?-galactosidase A, that produces accumulation of globotriaosylceramide. There is a multisystemic involvement, ...
CYP1A1 *2B and *4 polymorphisms are associated with lung cancer susceptibility in Mexican patients
(2008)
Background: CYP1A1 is a gene involved in the high aryl hydrocarbon hydroxylase -inducible phenotype, which is a genetically-determined variation among individuals that has been associated with lung cancer risk. More ...
Chromosomal abnormalities in patients with azoospermia in western Mexico
(2006)
? In order to assess the frequency of chromosomal abnormalities in azoospermic males from western Mexico, we carried out a retrospective study in 227 patients. Forty-three (18.9%) cases with an abnormal karyotype were ...