Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Kullasate Sakpichaisakul"'
Autor:
Kamornwan Katanyuwong, Utcharee Intusoma, Kullasate Sakpichaisakul, Tanitnun Paprad, Piradee Suwanpakdee, Chaiyos Khongkhatithum, Oranee Sanmaneechai
Publikováno v:
BMJ Paediatrics Open, Vol 8, Iss 1 (2024)
Objective To elucidate the clinical characteristics and standard of care (SoC) of spinal muscular atrophy (SMA) patients in Thailand, focusing on primary endpoints: age at death and a composite of death or tracheostomy need.Design Retrospective obser
Externí odkaz:
https://doaj.org/article/54ab785ec6314b049ea27a04a43f0ad5
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:
Thipwimol Tim-Aroon, Khunton Wichajarn, Kamornwan Katanyuwong, Pranoot Tanpaiboon, Nithiwat Vatanavicharn, Kullasate Sakpichaisakul, Arthaporn Kongkrapan, Jakris Eu-ahsunthornwattana, Supranee Thongpradit, Kanya Moolsuwan, Nusara Satproedprai, Surakameth Mahasirimongkol, Tassanee Lerksuthirat, Bhoom Suktitipat, Natini Jinawath, Duangrurdee Wattanasirichaigoon
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-9 (2021)
Abstract Background Sandhoff disease (SD) is an autosomal recessive lysosomal storage disorder, resulting in accumulation of GM2 ganglioside, particular in neuronal cells. The disorder is caused by deficiency of β-hexosaminidase B (HEX-B), due to pa
Externí odkaz:
https://doaj.org/article/5793a6bb9459425ea999df2f70d8699e
Autor:
Edward Yang, Sara Cherkerzian, Terrie E. Inder, Kullasate Sakpichaisakul, Mohamed El-Dib, Krittin J. Supapannachart, Eniko Szakmar, Julian N. Robinson, Brain H. Walsh, Joseph J. Volpe
Publikováno v:
Journal of Perinatology. 41:2261-2269
To correlate arterial umbilical cord gas (aUCG) and infant blood gas with severity of neurological injury. Retrospective single-site study of infants evaluated for therapeutic hypothermia. Clinical neurological examination and a validated MRI scoring
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6cebb495ba71c66b0bfa831ce9ffcccc
https://doi.org/10.1038/s41372-021-01075-w
https://doi.org/10.1038/s41372-021-01075-w
Autor:
Duangrurdee Wattanasirichaigoon, Natini Jinawath, Tassanee Lerksuthirat, Nithiwat Vatanavicharn, Nusara Satproedprai, Arthaporn Kongkrapan, Kamornwan Katanyuwong, Pranoot Tanpaiboon, Bhoom Suktitipat, Thipwimol Tim-Aroon, Surakameth Mahasirimongkol, Kanya Moolsuwan, Jakris Eu-ahsunthornwattana, Khunton Wichajarn, Supranee Thongpradit, Kullasate Sakpichaisakul
Publikováno v:
BMC Pediatrics, Vol 21, Iss 1, Pp 1-9 (2021)
BMC Pediatrics
BMC Pediatrics
Background Sandhoff disease (SD) is an autosomal recessive lysosomal storage disorder, resulting in accumulation of GM2 ganglioside, particular in neuronal cells. The disorder is caused by deficiency of β-hexosaminidase B (HEX-B), due to pathogenic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::da8d103f1855baeb62aecf039e196f7d
https://doaj.org/article/5793a6bb9459425ea999df2f70d8699e
https://doaj.org/article/5793a6bb9459425ea999df2f70d8699e
Autor:
Francesco T. Mangano, Anna W. Byars, Paul S. Horn, Ravindra Arya, Kullasate Sakpichaisakul, Gewalin Aungaroon, Katherine D. Holland, Hansel M. Greiner
Publikováno v:
Seizure. 80:183-191
Purpose We studied the association between electrical stimulation mapping (ESM) with a visual naming task and post-operative neuropsychological outcomes after pediatric epilepsy surgery. Methods Children who underwent epilepsy surgery, having pre- an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1a2bcfc3dcd178d441a6c3d07b2cdf71
https://doi.org/10.1016/j.seizure.2020.06.029
https://doi.org/10.1016/j.seizure.2020.06.029
Autor:
Kingthong Anurat, Piangor Watcharakuldilok, Kullasate Sakpichaisakul, Chaiyos Khongkhatithum, Surakameth Mahasirimongkol, Punna Kunhapan, Wimala Inunchot, Sukanya Wattanapokayakit, Orathai Munggaranonchai, Lunliya Thampratankul
Publikováno v:
Pediatric neurology. 134
Anti-N-methyl-d-aspartate receptor encephalitis (anti-NMDARE) is one of the most common types of autoimmune encephalitis. Most patients have no apparent immunologic triggers, which suggests a genetic predisposition. This study was conducted to identi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f33e2741e94248082988289f91550d1f
https://pubmed.ncbi.nlm.nih.gov/35863207
https://pubmed.ncbi.nlm.nih.gov/35863207
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