Publications by authors named "Objoon Trachoo"

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Generation of integration-free human induced pluripotent stem cell line MUi040-A derived from CD34 + hematopoietic stem cells of a patient with constitutional pericentric inversion of chromosome 9.
Aung Khine Linn, Phetcharat Phanthong, Yongyut Pewkliang, Wanida Laosee, Pirut Tong-Ngam, Objoon Trachoo

Stem Cell Res· December 2025

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Nationwide carrier screening for congenital adrenal hyperplasia: integrated approach of CYP21A2 pathogenic variant genotyping and comprehensive large gene deletion analysis.
Yossawat Suwanlikit, Bhakbhoom Panthan, Pawares Chitayanan, Sommon Klumsathian, Angkana Charoenyingwattana, Objoon Trachoo

BMC Med Genomics· January 2025

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Population-based FMR1 carrier screening among reproductive women.
Quratul Ain, Ye Hyun Hwang, Daryl Yeung, Pacharee Panpaprai, Wiwat Iamurairat, Objoon Trachoo

J Assist Reprod Genet· November 2024

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Successful Treatment of Schwartz-Jampel Syndrome with Botulinum Toxin Type A.
Panittra Suphatsathienkul, Kullasate Sakpichaisakul, Thanin Wechapinan, Objoon Trachoo, Sorawit Virawan

Dermatol Ther (Heidelb)· February 2024

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Epileptic spasms related to neuronal differentiation factor 2 (NEUROD2) mutation respond to combined vigabatrin and high dose prednisolone therapy.
Kullasate Sakpichaisakul, Rachata Boonkrongsak, Punjama Lertbutsayanukul, Nareenart Iemwimangsa, Sommon Klumsathian, Objoon Trachoo

BMC Neurol· December 2022

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Genomic findings of hypertrophic and dilated cardiomyopathy characterized in a Thai clinical genetics service.
Objoon Trachoo, Teerapat Yingchoncharoen, Tawai Ngernsritrakul, Nareenart Iemwimangsa, Bhakbhoom Panthan

PLoS One· September 2022

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Amelioration of osteogenesis in iPSC-derived mesenchymal stem cells from osteogenesis imperfecta patients by endoplasmic reticulum stress inhibitor.
Thitinat Duangchan, Tulyapruek Tawonsawatruk, Chanika Angsanuntsukh, Objoon Trachoo, Suradej Hongeng

Life Sci· August 2021

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Clinical utility of combined preimplantation genetic testing methods in couples at risk of passing on beta thalassemia/hemoglobin E disease: A retrospective review from a single center.
Chonthicha Satirapod, Matchuporn Sukprasert, Bhakbhoom Panthan, Angkana Charoenyingwattana, Pawares Chitayanan, Objoon Trachoo

PLoS One· March 2020

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Novel PANK2 mutation discovered among South East Asian children living in Thailand affected with pantothenate kinase associated neurodegeneration.
Kullasate Sakpichaisakul, Vitchayaporn E Saengow, Papit Suwanpratheep, Kanokpan Rongnoparat, Bhakbhoom Panthan, Objoon Trachoo

J Clin Neurosci· August 2019

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Oral manifestations in patients and dogs with mucopolysaccharidosis Type VII.
Piranit N Kantaputra, Lachlan J Smith, Margret L Casal, Chulaluck Kuptanon, Yu-Cheng Chang, Objoon Trachoo

Am J Med Genet A· March 2019

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Clinical course over five decades of a woman carrying 16p13.3 microduplication.
Sarunpong Pibalyart, Objoon Trachoo

Clin Dysmorphol· October 2017

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Exome sequencing for simultaneous mutation screening in children with hemophagocytic lymphohistiocytosis.
Ekchol Mukda, Objoon Trachoo, Ekawat Pasomsub, Rawiphorn Tiyasirichokchai, Nareenart Iemwimangsa

Int J Hematol· August 2017

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A Novel Mutation Identified in a Patient with Isolated Primary Pigmented Nodular Adrenocortical Disease.
Sira Korpaisarn, Objoon Trachoo, Bhakbhoom Panthan, Rangsima Aroonroch, Ronnarat Suvikapakornkul

Case Rep Oncol· August 2017

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Low oxygen saturation and severe anemia in compound heterozygous Hb Louisville [β42(CD1)Phe→Leu] and Hb La Desirade [β129(H7)Ala→Val].
Parin Kamseng, Satariya Trakulsrichai, Objoon Trachoo, Walaiporn Yimniam, Bhakbhoom Panthan

Hematology· March 2017

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First successful trial of preimplantation genetic diagnosis for pantothenate kinase-associated neurodegeneration.
Objoon Trachoo, Chonthicha Satirapod, Bhakbhoom Panthan, Matchuporn Sukprasert, Angkana Charoenyingwattana

J Assist Reprod Genet· January 2017

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Screening of Fabry disease in patients with end-stage renal disease of unknown etiology: the first Thailand study.
Objoon Trachoo, Paisan Jittorntam, Sarunpong Pibalyart, Saowanee Kajanachumphol, Norasak Suvachittanont

J Biomed Res· October 2016

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FIRST IDENTIFICATION OF HEMOGLOBIN LANSINGRAMATHIBODI [α87(F8)His → Gln; CAC>CAG (HBA1: c.264C>G)] IN A THAI FAMILY WITH SPURIOUS HYPOXEMIA.
Satariya Trakulsrichai, Bhakbhoom Panthan, Paisan Jittorntam, Pimjai Niparuck, Charuwan Sriapha, Objoon Trachoo

Southeast Asian J Trop Med Public Health· September 2016

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Angiotensin-converting enzyme gene polymorphism in Thai patients with systemic lupus erythematosus.
Umporn Pitipakorn, Parawee Suwannalai, Objoon Trachoo, Sasivimol Rattanasiri, Sermsiri Chitphuk

Int J Rheum Dis· July 2016

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A Novel Mutation in Thyroid Peroxidase Gene Causing Congenital Goitrous Hypothyroidism in a German-Thai Patient.
Chutintorn Sriphrapradang, Yotsapon Thewjitcharoen, Suwannee Chanprasertyothin, Soontaree Nakasatien, Thep Himathongkam, Objoon Trachoo

J Clin Res Pediatr Endocrinol· June 2016

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Fine-needle aspiration cytology of parathyroid carcinoma mimic hürthle cell thyroid neoplasm.
Chutintorn Sriphrapradang, Pattana Sornmayura, Niramol Chanplakorn, Objoon Trachoo, Pattarana Sae-Chew

Case Rep Endocrinol· September 2014

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Chromosome 20p inverted duplication deletion identified in a Thai female adult with mental retardation, obesity, chronic kidney disease and characteristic facial features.
Objoon Trachoo, Montira Assanatham, Natini Jinawath, Arkom Nongnuch

Eur J Med Genet· June 2013

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Chromosome 22q11.2 deletion syndrome presenting as adult onset hypoparathyroidism: clues to diagnosis from dysmorphic facial features.
Sira Korpaisarn, Objoon Trachoo, Chutintorn Sriphrapradang

Case Rep Endocrinol· June 2013

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A genetic association study between growth differentiation factor 5 (GDF 5) polymorphism and knee osteoarthritis in Thai population.
Tulyapruek Tawonsawatruk, Theeraroj Changthong, Sarinee Pingsuthiwong, Objoon Trachoo, Thanyachai Sura

J Orthop Surg Res· September 2011

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Noonan syndrome, metabolic syndrome and stroke-in-the-young: coincidence, causal or contribution?
Jakris Eu-ahsunthornwattana, Objoon Trachoo, Donniphat Dejsuphong, Atchara Tunteeratum, Kanoknan Srichan

J Med Assoc Thai· September 2010

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Association of estrogen receptor-alpha single-nucleotide polymorphism (codon 594 G-->A) and Thai patients affected by knee osteoarthritis.
Tulyapruek Tawonsawatruk, Objoon Trachoo, Thanaphot Channoom, Thanyachai Sura, Jakris Eu-ahsunthornwattana

J Med Assoc Thai· December 2009

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