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Catherine Lynn T Silao

Showing results (1-10 of 13) with videos related to

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Nestle Nutrition Institute Workshop Series|April 6, 2023
A Child's Nutrition and EpigeneticsCatherine Lynn T Silao
Molecular Genetics and Metabolism|January 27, 2004
A novel deletion creating a new terminal exon of the dihydrolipoyl transacylase gene is a founder mutation of Filipino maple syrup urine diseaseCatherine Lynn T Silao, Carmencita D Padilla, Masafumi Matsuo
Pediatrics International : Official Journal of the Japan Pediatric Society|June 7, 2008
Early diagnosis of maple syrup urine disease using polymerase chain reaction-based mutation detectionCatherine Lynn T Silao, Carmencita D Padilla, Masafumi Matsuo
The Kobe Journal of Medical Sciences|September 19, 2013
Mutational analysis of the GALT gene in Filipino patientsSylvia C Estrada, Daffodil M Canson, Catherine Lynn T Silao
JIMD Reports|August 9, 2019
Functional analysis of <i>GALT</i> variants found in classic galactosemia patients using a novel cell-free translation methodDaffodil M Canson, Catherine Lynn T Silao, Salvador Eugenio C Caoili
Acta Medica Philippina|February 19, 2025
Association of <i>TP53</i> Germline Variant and Choledochal Cyst among Clinically Diagnosed Filipino Pediatric PatientsDanna Mae S Opiso, Germana Emerita V Gregorio, Catherine Lynn T Silao
Pediatrics International : Official Journal of the Japan Pediatric Society|May 6, 2015
Novel cystathionine β-synthase gene mutations in a Filipino patient with classic homocystinuriaCatherine Lynn T Silao, Terence Diane F Fabella, Kahlil Izza D Rama, et al.
Saudi Medical Journal|April 20, 2025
Advancing genetic counselling in Southern Africa: Unveiling opportunities for inclusive healthcare and genomic education for AngolaMaria Chimpolo, Shahida Moosa, Catherine Lynn T Silao, et al.
Orphanet Journal of Rare Diseases|January 13, 2017
Clinical, biochemical and molecular characteristics of Filipino patients with mucopolysaccharidosis type II - Hunter syndromeMary Anne D Chiong, Daffodil M Canson, Mary Ann R Abacan, et al.
Acta Medica Philippina|September 23, 2024
Caring Behavior of Filipinos toward their Elderly Family MembersEva Belingon Felipe-Dimog, Ma-Am Joy Realce Tumulak, Angely P Garcia, et al.
Pageof 2

Showing results (1-10 of 13) with videos related to

Sort By:
Pageof 2
Nestle Nutrition Institute Workshop Series|April 6, 2023
A Child's Nutrition and EpigeneticsCatherine Lynn T Silao
Molecular Genetics and Metabolism|January 27, 2004
A novel deletion creating a new terminal exon of the dihydrolipoyl transacylase gene is a founder mutation of Filipino maple syrup urine diseaseCatherine Lynn T Silao, Carmencita D Padilla, Masafumi Matsuo
Pediatrics International : Official Journal of the Japan Pediatric Society|June 7, 2008
Early diagnosis of maple syrup urine disease using polymerase chain reaction-based mutation detectionCatherine Lynn T Silao, Carmencita D Padilla, Masafumi Matsuo
The Kobe Journal of Medical Sciences|September 19, 2013
Mutational analysis of the GALT gene in Filipino patientsSylvia C Estrada, Daffodil M Canson, Catherine Lynn T Silao
JIMD Reports|August 9, 2019
Functional analysis of <i>GALT</i> variants found in classic galactosemia patients using a novel cell-free translation methodDaffodil M Canson, Catherine Lynn T Silao, Salvador Eugenio C Caoili
Acta Medica Philippina|February 19, 2025
Association of <i>TP53</i> Germline Variant and Choledochal Cyst among Clinically Diagnosed Filipino Pediatric PatientsDanna Mae S Opiso, Germana Emerita V Gregorio, Catherine Lynn T Silao
Pediatrics International : Official Journal of the Japan Pediatric Society|May 6, 2015
Novel cystathionine β-synthase gene mutations in a Filipino patient with classic homocystinuriaCatherine Lynn T Silao, Terence Diane F Fabella, Kahlil Izza D Rama, et al.
Saudi Medical Journal|April 20, 2025
Advancing genetic counselling in Southern Africa: Unveiling opportunities for inclusive healthcare and genomic education for AngolaMaria Chimpolo, Shahida Moosa, Catherine Lynn T Silao, et al.
Orphanet Journal of Rare Diseases|January 13, 2017
Clinical, biochemical and molecular characteristics of Filipino patients with mucopolysaccharidosis type II - Hunter syndromeMary Anne D Chiong, Daffodil M Canson, Mary Ann R Abacan, et al.
Acta Medica Philippina|September 23, 2024
Caring Behavior of Filipinos toward their Elderly Family MembersEva Belingon Felipe-Dimog, Ma-Am Joy Realce Tumulak, Angely P Garcia, et al.
Pageof 2