Diana Cruz-Garcia

Instituto De Genética Humana Dr. Enrique Corona Rivera
Guadalajara, JAL, Mexico

Last Updated: 09/26/2026

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Found 13 publications

VNTR of the ATXN2 gene as a biomarker of thrombophlebitis in patients with type 2 diabetes and COVID-19.

VNTR of the ATXN2 gene as a biomarker of thrombophlebitis in patients with type 2 diabetes and COVID-19.

Journal: Cirugia y cirujanos

Published: May 31, 2022

Alta frecuencia del alelo ancestral del polimorfismo SNV rs11212617 del gen ATM en población mestiza mexicana del Noroccidente.

Alta frecuencia del alelo ancestral del polimorfismo SNV rs11212617 del gen ATM en población mestiza mexicana del Noroccidente.

Journal: Cirugia y cirujanos

Published: March 29, 2022

A FEMALE CASE OF SPINOCEREBELLAR ATAXIA TYPE 10 WITH SUICIDAL BEHAVIOR AND ENDOCRINPATHIES ASSOCIATED WITH A MASSIVE EXPANSION (ATTCT) OF THE GENE ATXN10.

A FEMALE CASE OF SPINOCEREBELLAR ATAXIA TYPE 10 WITH SUICIDAL BEHAVIOR AND ENDOCRINPATHIES ASSOCIATED WITH A MASSIVE EXPANSION (ATTCT) OF THE GENE ATXN10.

Journal: Actas espanolas de psiquiatria

Published: January 01, 2022

Alteraciones de la coagulación y marcadores de trombofilia en un paciente con SARS-CoV-2, diabetes tipo 2, hipotiroidismo y flebitis de miembro pélvico izquierdo.

Alteraciones de la coagulación y marcadores de trombofilia en un paciente con SARS-CoV-2, diabetes tipo 2, hipotiroidismo y flebitis de miembro pélvico izquierdo.

Journal: Cirugia y cirujanos

Published: August 05, 2021

A clinical report of the massive CAG repeat expansion in spinocerebellar ataxia type 2: Severe onset in a Mexican child and review previous cases.

A clinical report of the massive CAG repeat expansion in spinocerebellar ataxia type 2: Severe onset in a Mexican child and review previous cases.

Journal: Genetics and molecular biology

Published: October 12, 2019

Recurrent achondrogenesis type 1A1 is due to allelic variant of the COL10A1 genéCOL10A1?

Recurrent achondrogenesis type 1A1 is due to allelic variant of the COL10A1 genéCOL10A1?

Journal: Cirugia y cirujanos

Published: August 27, 2019

New subtype of familial achondrogenesis type IA (Houston-Harris).

New subtype of familial achondrogenesis type IA (Houston-Harris).

Journal: Cirugia y cirujanos

Published: April 06, 2019

New subtype of familial achondrogenesis type IA (Houston-Harris).

New subtype of familial achondrogenesis type IA (Houston-Harris).

Journal: Cirugia y cirujanos

Published: April 24, 2018

Epidemiología genética sobre las teorías causales y la patogénesis de la diabetes mellitus tipo 2.

Epidemiología genética sobre las teorías causales y la patogénesis de la diabetes mellitus tipo 2.

Journal: Gaceta medica de Mexico

Published: February 08, 2018

(CAG)n polymorphism of the ATXN2 gene, a new marker of susceptibility for type 2 diabetes mellitus

(CAG)n polymorphism of the ATXN2 gene, a new marker of susceptibility for type 2 diabetes mellitus

Journal: Revista panamericana de salud publica = Pan American journal of public health

Published: December 02, 2015

Anterior cervical hypertrichosis: case report

Anterior cervical hypertrichosis: case report

Journal: Archivos argentinos de pediatria

Published: October 21, 2015

Ethical considerations in presymptomatic diagnosis of autosomal dominant spinocerebellar ataxias.

Ethical considerations in presymptomatic diagnosis of autosomal dominant spinocerebellar ataxias.

Journal: Neurologia (Barcelona, Spain)

Published: December 18, 2014

Showing 1-12 of 13

Last Updated: 09/26/2026