Unusual presentation as an adult onset painful myopathy in a Thai patient with Becker muscular dystrophy.

بواسطة Manop Pithukpakorn
منشور في 2018

Clinical presentation and echocardiographic findings of Thai patients with Marfan syndrome

بواسطة Manop Pithukpakorn, Nithima Chaowalit
منشور في 2018

Physician awareness, preparedness, and opinions toward consumer-initiated genetic testing in Thailand: Views from a changing landscape

بواسطة Siraphob Kittikoon, Manop Pithukpakorn, Pornpoj Pramyothin
منشور في 2022

A 47, XXY patient and Xq21.31 duplication with features of Prader-Willi syndrome: Results of array-based comparative genomic hybridization

بواسطة Pornpoj Pramyothin, Manop Pithukpakorn, Richard F. Arakaki
منشور في 2018

HLA-B*27:04 associated with enthesitis and younger age of onset, and HLA-B allele profile in patients with ankylosing spondylitis in Thailand: A cross-sectional study

بواسطة Praveena Chiowchanwisawakit, Manop Pithukpakorn, Komon Luangtrakool, Parichart Permpikul
منشور في 2022

Successful treatment of arrhythmia with β-blocker and flecainide combination in pregnant patients with Andersen–Tawil syndrome: A case report and literature review

بواسطة Pongprueth Rujirachun, Apichaya Junyavoraluk, Manop Pithukpakorn, Bhoom Suktitipat, Arjbordin Winijkul
منشور في 2020

Germline ATM mutation and somatic PIK3CA and BCOR mutations found in an infant with aggressive orbital embryonal rhabdomyosarcoma

بواسطة Pimkwan Jaru-ampornpan, Chottiwat Tansirisithikul, Manachaya Prukajorn, Somponnat Sampattavanich, Manop Pithukpakorn
منشور في 2022

Precision medicine in Thailand

بواسطة Vorasuk Shotelersuk, Sissades Tongsima, Manop Pithukpakorn, Jakris Eu-ahsunthornwattana, Surakameth Mahasirimongkol
منشور في 2020

Identification of novel mutation in RANKL by whole-exome sequencing in a Thai family with osteopetrosis; a case report and review of RANKL osteopetrosis

بواسطة Pongtawat Lertwilaiwittaya, Bhoom Suktitipat, Phongphak Khongthon, Warut Pongsapich, Chanin Limwongse, Manop Pithukpakorn
منشور في 2022

A novel mutation of the GNE gene in distal myopathy with rimmed vacuoles: A case with inflammation

بواسطة Jantima Tanboon, Kanjana Rongsa, Manop Pithukpakorn, Kanokwan Boonyapisit, Chanin Limwongse, Tumtip Sangruchi
منشور في 2018

Novel mutation of the TINF2 gene in a patient with dyskeratosis congenita

بواسطة Benjaporn Panichareon, Thanawat Seedapan, Wanna Thongnoppakhun, Chanin Limwongse, Manop Pithukpakorn, Thawornchai Limjindaporn
منشور في 2018

Meta-analysis of the plasminogen activator inhibitor-1 (PAI-1) gene with insertion/deletion 4G/5G polymorphism and its susceptibility to ischemic stroke in Thai population

بواسطة Anunchai Assawamakin, Narin Sriratanaviriyakul, Yupaporn Lalerd, Wanna Thongnoppakhun, Oranud Praditsap, Sissades Tongsima, Manop Pithukpakorn
منشور في 2018

Mycophenolic acid AUC in Thai kidney transplant recipients receiving low dose mycophenolate and its association with UGT2B7 polymorphisms

بواسطة Manop Pithukpakorn, Tiwat Tiwawanwong, Yupaporn Lalerd, Anunchai Assawamakin, Nalinee Premasathian, Adis Tasanarong, Wanna Thongnoppakhun, Attapong Vongwiwatana
منشور في 2018

Clinical outcome and laboratory markers for predicting disease activity in patients with disseminated opportunistic infections associated with anti-interferon-γ autoantibodies

بواسطة Nasikarn Angkasekwinai, Yupin Suputtamongkol, Pakpoom Phoompoung, Manop Pithukpakorn, Ekkarat Wongswat, Pinklow Umrod, Sasima Tongsai, Suporn Foongladda
منشور في 2020

Six novel ATP7B mutations in Thai patients with Wilson disease

بواسطة Benjaporn Panichareon, Krailerk Taweechue, Wanna Thongnoppakhun, Monthikan Aksornworanart, Manop Pithukpakorn, Pa thai Yenchitsomanus, Chanin Limwongse, Thawornchai Limjindaporn
منشور في 2018

Molecular investigation by whole exome sequencing revealed a high proportion of pathogenic variants among Thai victims of sudden unexpected death syndrome

بواسطة Bhoom Suktitipat, Sakda Sathirareuangchai, Ekkapong Roothumnong, Wanna Thongnoppakhun, Purin Wangkiratikant, Nutchavadee Vorasan, Rungroj Krittayaphong, Manop Pithukpakorn, Warangkna Boonyapisit
منشور في 2018

Factors associated with acquired Anti IFN- γ autoantibody in patients with nontuberculous mycobacterial infection

بواسطة Pakpoom Phoompoung, Nasikarn Ankasekwinai, Manop Pithukpakorn, Suporn Foongladda, Pinklow Umrod, Bhoom Suktitipat, Surakameth Mahasirimongkol, Sasisopin Kiertiburanakul, Yupin Suputtamongkol
منشور في 2018

High frequency of KRAS codon 146 and FBXW7 mutations in Thai patients with stage II-III colon cancer

بواسطة Krittiya Korphaisarn, Ananya Pongpaibul, Ekkapong Roothumnong, Khontawan Pongsuktavorn, Lucksamon Thamlikitkul, Tauangtham Anekpuritanang, Naravat Poungvarin, Wanna Thongnoppakhun, Manop Pithukpakorn
منشور في 2020

Derivation of an induced pluripotent stem cell line (MUSIi004-A) from dermal fibroblasts of a 48-year-old spinocerebellar ataxia type 3 patient

بواسطة Alisa Ritthaphai, Methichit Wattanapanitch, Manop Pithukpakorn, Worapa Heepchantree, Rungtip Soi-ampornkul, Panchalee Mahaisavariya, Daranporn Triwongwaranat, Kovit Pattanapanyasat, Chinnavuth Vatanashevanopakorn
منشور في 2019

HLA-DRB1 and HLA-DQB1 are associated with adult-onset immunodeficiency with acquired anti-interferon-gamma autoantibodies

بواسطة Manop Pithukpakorn, Ekkapong Roothumnong, Nasikarn Angkasekwinai, Bhoom Suktitipat, Anunchai Assawamakin, Voravich Luangwedchakarn, Pinklow Umrod, Wanna Thongnoppakhun, Suporn Foongladda, Yupin Suputtamongkol
منشور في 2018