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Journal of the Endocrine Society|January 9, 2019
Identification and Functional Analysis of Six DAX1 Mutations in Patients With X-Linked Adrenal Hypoplasia CongenitaChanisara Suthiworachai, Rachaneekorn Tammachote, Chalurmpon Srichomthong, et al.
Genes & Genomics|August 30, 2018
rs11567842 SNP in SLC13A2 gene associates with hypocitraturia in Thai patients with nephrolithiasisPattarin Udomsilp, Sarawut Saepoo, Rungnapa Ittiwut, et al.
European Journal of Haematology|September 10, 2017
Novel mutations in Thai patients with glanzmann thrombastheniaRungnapa Ittiwut, Pintip Suchartlikitwong, Yaowaree Kittikalayawong, et al.
Scientific Reports|January 16, 2023
Pathogenic variant detection rate by whole exome sequencing in Thai patients with biopsy-proven focal segmental glomerulosclerosisSuramath Isaranuwatchai, Ankanee Chanakul, Chupong Ittiwut, et al.
Emerging Infectious Diseases|October 3, 2022
TIGIT Monoallelic Nonsense Variant in Patient with Severe COVID-19 Infection, ThailandPimpayao Sodsai, Chupong Ittiwut, Vichaya Ruenjaiman, et al.
Clinical Genetics|August 21, 2024
Novel PLEC variants associated with infantile cholestasisPhawin Kor-Anantakul, Huey-Ling Chen, Ya-Hui Chen, et al.
Journal of Clinical Pathology|December 6, 2023
Genetic variations of type 2 and type 3 von Willebrand diseases in ThailandSupanun Lauhasurayotin, Chatphatai Moonla, Rungnapa Ittiwut, et al.
European Journal of Human Genetics : EJHG|October 5, 2022
Exome sequencing as first-tier genetic testing in infantile-onset pharmacoresistant epilepsy: diagnostic yield and treatment impactPonghatai Boonsimma, Chupong Ittiwut, Wuttichart Kamolvisit, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|April 8, 2025
Two distinct phenotypes and a novel mutation in limb-girdle muscular dystrophy R7 telethonin-related patients from Thai neuromuscular centerTanitnun Paprad, Jakkrit Amornvit, Thippamas Pobsuk, et al.
American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics|June 10, 2011
Association between polymorphisms in catechol-O-methyltransferase (COMT) and cocaine-induced paranoia in European-American and African-American populationsRungnapa Ittiwut, Jennifer B Listman, Chupong Ittiwut, et al.
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