Alfredo Rodriguez-Santana

Las Palmas De Gran Canaria, CN, Spain

Last Updated: 09/26/2026

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Found 12 publications

Whole genome methylation profiling of menstrual stem cells identifies novel biomarkers for endometriosis.

Whole genome methylation profiling of menstrual stem cells identifies novel biomarkers for endometriosis.

Journal: Communications medicine
Published: September 12, 2025

Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction.

Role of TBX20 Truncating Variants in Dilated Cardiomyopathy and Left Ventricular Noncompaction.

Journal: Circulation. Genomic and precision medicine
Published: February 14, 2024

Prenatal diagnosis of Greig Cephalopolysyndactyly Syndrome. When to suspect it.

Prenatal diagnosis of Greig Cephalopolysyndactyly Syndrome. When to suspect it.

Journal: The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians
Published: June 05, 2020

Congenital hyperinsulinism in Gran Canaria, Canary Isles.

Congenital hyperinsulinism in Gran Canaria, Canary Isles.

Journal: Anales de pediatria
Published: April 08, 2020

The solitary median maxillary central incisor (SMMCI) syndrome: Associations, prenatal diagnosis, and outcomes.

The solitary median maxillary central incisor (SMMCI) syndrome: Associations, prenatal diagnosis, and outcomes.

Journal: Prenatal diagnosis
Published: August 23, 2018

X-linked adrenal hypoplasia congenita: Novel missense mutation of DAX-1 gene.

X-linked adrenal hypoplasia congenita: Novel missense mutation of DAX-1 gene.

Journal: Medicina clinica
Published: April 25, 2018

Aicardi-Goutieres syndrome due to mutation of the IFIH1 gene with pontine involvement. A case report

Aicardi-Goutieres syndrome due to mutation of the IFIH1 gene with pontine involvement. A case report

Journal: Revista de neurologia
Published: September 24, 2016

Evaluation of family history of permanent hearing loss in childhood as a risk indicator in universal screening.

Evaluation of family history of permanent hearing loss in childhood as a risk indicator in universal screening.

Journal: Acta otorrinolaringologica espanola
Published: April 17, 2016

X-linked hereditary spastic paraplegia due to mutation in the L1CAM gene: three cases reports of CRASH syndrome

X-linked hereditary spastic paraplegia due to mutation in the L1CAM gene: three cases reports of CRASH syndrome

Journal: Revista de neurologia
Published: February 27, 2016

Three cases of Pallister-Killian syndrome

Three cases of Pallister-Killian syndrome

Journal: Revista de neurologia
Published: January 09, 2014

Stem cells protect the bronchial stump in rat, increasing Sox6, Col2a1, and Agc1 expression.

Stem cells protect the bronchial stump in rat, increasing Sox6, Col2a1, and Agc1 expression.

Journal: Lung
Published: July 25, 2013

Familial hemiplegic migraine type 2: two paediatric case reports

Familial hemiplegic migraine type 2: two paediatric case reports

Journal: Revista de neurologia
Published: February 09, 2012
Showing 1-12 of 12

Last Updated: 09/26/2026