Zobrazeno 1 - 10
of 38
pro vyhledávání: '"Objoon Trachoo"'
Autor:
Panittra Suphatsathienkul, Kullasate Sakpichaisakul, Thanin Wechapinan, Objoon Trachoo, Sorawit Virawan, Rungsima Wanitphakdeedecha
Publikováno v:
Dermatology and Therapy, Vol 14, Iss 2, Pp 545-556 (2024)
Abstract Schwartz-Jampel syndrome (SJS) is a rare autosomal recessive disorder characterized by typical facial dysmorphism, generalized muscle stiffness, joint contracture, and skeletal abnormalities. This condition is caused by mutations in the hepa
Externí odkaz:
https://doaj.org/article/8856e5a2577c44798389ed35da09208d
Autor:
Kullasate Sakpichaisakul, Rachata Boonkrongsak, Punjama Lertbutsayanukul, Nareenart Iemwimangsa, Sommon Klumsathian, Bhakbhoom Panthan, Objoon Trachoo
Publikováno v:
BMC Neurology, Vol 22, Iss 1, Pp 1-9 (2022)
Abstract Background Epileptic spasms are a devastating form of early infantile epileptic encephalopathy (EIEE) with various etiologies. Early diagnosis and a shorter lead time to treatment are crucial to stop the seizures and optimize the neurodevelo
Externí odkaz:
https://doaj.org/article/632b28ad91124c08be8dd0b40cdbba96
Autor:
Objoon Trachoo, Teerapat Yingchoncharoen, Tawai Ngernsritrakul, Nareenart Iemwimangsa, Bhakbhoom Panthan, Sommon Klumsathian, Sasima Srisukh, Anucha Mukdadilok, Sithakom Phusanti, Angkana Charoenyingwattana, Takol Chareonsirisuthigul, Wasun Chantratita, Tarinee Tangcharoen
Publikováno v:
PLoS ONE, Vol 17, Iss 9 (2022)
Hypertrophic cardiomyopathy (HCM) and dilated cardiomyopathy (DCM) are the most common referrals in the Inherited Cardiovascular Condition (ICC) Genetics Service. Several issues must be discussed with patients and their families during the genetic co
Externí odkaz:
https://doaj.org/article/eeae5b44c0734ee4ab85b0a57b726c10
Autor:
Sira Korpaisarn, Objoon Trachoo, Bhakbhoom Panthan, Rangsima Aroonroch, Ronnarat Suvikapakornkul, Chutintorn Sriphrapradang
Publikováno v:
Case Reports in Oncology, Vol 10, Iss 2, Pp 769-776 (2017)
Primary pigmented nodular adrenocortical disease (PPNAD) is a rare cause of Cushing syndrome, especially the isolated form without Carney complex, associated with germline mutations in PRKAR1A, the protein kinase A regulatory subunit type 1 alpha gen
Externí odkaz:
https://doaj.org/article/002b73c3810f45ea8e8e277e0cf041bb
Autor:
Chonthicha Satirapod, Matchuporn Sukprasert, Bhakbhoom Panthan, Angkana Charoenyingwattana, Pawares Chitayanan, Wasun Chantratita, Wicharn Choktanasiri, Objoon Trachoo, Suradej Hongeng
Publikováno v:
PLoS ONE, Vol 14, Iss 11, p e0225457 (2019)
Thalassemia and hemoglobinopathy is a group of hereditary blood disorder with diverse clinical manifestation inherited by autosomal recessive manner. The Beta thalassemia/Hemoglobin E disease (HbE/βthal) causes a variable degree of hemolysis and the
Externí odkaz:
https://doaj.org/article/582ef307c1b04453a060f9206bcfa883
Autor:
Chutintorn Sriphrapradang, Pattana Sornmayura, Niramol Chanplakorn, Objoon Trachoo, Pattarana Sae-Chew, Rangsima Aroonroch
Publikováno v:
Case Reports in Endocrinology, Vol 2014 (2014)
Background. Fine-needle aspiration (FNA) can cause misdiagnosis of cytomorphological findings between parathyroid and thyroid lesions. Case Presentation. A 31-year-old man presented with a palpable neck mass on the right thyroid lobe. FNA cytology wa
Externí odkaz:
https://doaj.org/article/164fc5b3c2a04b3192a76d15342aaa53
Publikováno v:
Case Reports in Endocrinology, Vol 2013 (2013)
We report a 26-year-old Thai man who presented with hypoparathyroidism in adulthood. He had no history of cardiac disease and recurrent infection. His subtle dysmorphic facial features and mild intellectual impairment were suspected for chromosome 22
Externí odkaz:
https://doaj.org/article/4d9583cbbbf7400d955aef550349aafe
Autor:
Kullasate Sakpichaisakul, Rachata Boonkrongsak, Punjama Lertbutsayanukul, Nareenart Iemwimangsa, Sommon Klumsathian, Bhakbhoom Panthan, Objoon Trachoo
Publikováno v:
BMC neurology. 22(1)
Background Epileptic spasms are a devastating form of early infantile epileptic encephalopathy (EIEE) with various etiologies. Early diagnosis and a shorter lead time to treatment are crucial to stop the seizures and optimize the neurodevelopmental o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5bc2f1dcd5597519cf50a35ad179a1a5
https://pubmed.ncbi.nlm.nih.gov/36494631
https://pubmed.ncbi.nlm.nih.gov/36494631
Autor:
Bhakbhoom Panthan, Kanokpan Rongnoparat, Kullasate Sakpichaisakul, Papit Suwanpratheep, Objoon Trachoo, Vitchayaporn E. Saengow
Publikováno v:
Journal of Clinical Neuroscience. 66:187-190
Pantothenate kinase-associated neurodegeneration (PKAN) is linked to brain iron accumulation caused by PANK2 gene mutation. Despite the importance of genetic testing to confirm PKAN and identify at risk parents, genetic screening is financially burde
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::41162a7d7520a7af21da7e41887b9a70
https://doi.org/10.1016/j.jocn.2019.04.017
https://doi.org/10.1016/j.jocn.2019.04.017