Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Oranee Sanmaneechai"'
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
Survival analysis and life expectancy of pediatric patients with spinal muscular atrophy in Thailand
Publikováno v:
Heliyon, Vol 10, Iss 11, Pp e32732- (2024)
Background: Survival data for Thai patients with 5q spinal muscular atrophy (SMA), the leading cause of infant mortality worldwide, are lacking. Objective: This study aimed to determine the survival rates and life expectancies of pediatric patients w
Externí odkaz:
https://doaj.org/article/757f52c8c7e740fb864fc261041f1bb1
Autor:
Sarinya Summa, Chupong Ittiwut, Pimchanok Kulsirichawaroj, Tanitnun Paprad, Surachai Likasitwattanakul, Oranee Sanmaneechai, Ponghatai Boonsimma, Kanya Suphapeetiporn, Vorasuk Shotelersuk
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-7 (2023)
Abstract Muscular dystrophies and congenital myopathies are heterogeneous groups of inherited muscular disorders. An accurate diagnosis is challenging due to their complex clinical presentations and genetic heterogeneity. This study aimed to determin
Externí odkaz:
https://doaj.org/article/257deb5fa9a54799986dee357b92530d
Publikováno v:
Pediatrics and Neonatology, Vol 63, Iss 3, Pp 291-297 (2022)
Background: Spinal muscular atrophy (SMA) is a chronic genetic disease that causes varying degrees of disability. There is currently no data specific to the health-related quality of life (HRQoL) of Thai children and adolescents with SMA. Accordingly
Externí odkaz:
https://doaj.org/article/33813962a7084abc895a403a759644bd
Publikováno v:
Health and Quality of Life Outcomes, Vol 18, Iss 1, Pp 1-7 (2020)
Abstract Background Neuromuscular disorders (NMDs) are chronic illnesses that adversely impact the lives of patients and their families. The Pediatric Quality of Life™ 3.0 Neuromuscular Module (PedsQL™ 3.0 NMM) was designed to assess health-relat
Externí odkaz:
https://doaj.org/article/5ec055f35aa74df59acdbedbc2cc96ea
Publikováno v:
Health and Quality of Life Outcomes, Vol 17, Iss 1, Pp 1-8 (2019)
Abstract Background Duchenne Muscular Dystrophy (DMD) is the most common genetic neuromuscular disorder in children. This chronic illness may impact the physical, family, social and school life of affected children and their families. These impacts c
Externí odkaz:
https://doaj.org/article/95776589200b41bba5b5515e93fc6959
Publikováno v:
Siriraj Medical Journal, Vol 72, Iss 2 (2020)
Objective: There are no epidemiological data on childhood neuromuscular diseases in Thailand. We aimed to estimate the proportion of NMDs among pediatric neurology patients in Siriraj Hospital and determine the specific diagnosis. Methods: A retrospe
Externí odkaz:
https://doaj.org/article/0fad1ddb9a8341b3bc584bdf0c2dfd92
Autor:
Pimchanok Kulsirichawaroj, Oranee Sanmaneechai, Orasri Wittawatmongkol, Kulkanya Chokephaibulkit
Publikováno v:
Vaccines, Vol 10, Iss 1, p 134 (2022)
A 16-year-old Thai girl developed right facial palsy, a lower motor neuron lesion, and numbness 3 h after receiving the first dose of the BNT162b2 mRNA vaccine. Neurological examination showed the involvement of the right cranial nerves (CN) V, VII,
Externí odkaz:
https://doaj.org/article/f98170b281dd436cb0f8901bd8e47c9b
Autor:
Apirada Thongsing, Theeraphong Pho-iam, Chanin Limwongse, Surachai Likasitwattanakul, Oranee Sanmaneechai
Publikováno v:
eNeurologicalSci, Vol 16, Iss , Pp - (2019)
Case series reports on clinical features of pediatric hereditary neuropathy in Thailand is scarce. Subtype and clinical presentation in childhood-onset CMT differ from adult-onset. The aim of this study is to investigate the CMT phenotype in Thai chi
Externí odkaz:
https://doaj.org/article/a8c1e6cbc610491e9589812541501936
Autor:
Patra Yeetong, Pimchanok Kulsirichawaroj, Theerawat Kumutpongpanich, Chalurmpon Srichomthong, Phichittra Od-ek, Supphakorn Rakwongkhachon, Titaporn Thamcharoenvipas, Oranee Sanmaneechai, Monnat Pongpanich, Vorasuk Shotelersuk
Publikováno v:
Neuromuscular Disorders.