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Sunartini

Showing results (11-20 of 19) with videos related to

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BMC Proceedings|January 1, 2020
Use of air stacking to improve pulmonary function in Indonesian Duchenne muscular dystrophy patients: bridging the standard of care gap in low middle income country settingKristy Iskandar, Sunartini, Andika Priamas Nugrahanto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 28, 2024
Multidisciplinary approach on divergent outcomes in spinal muscular atrophies: comparing DYNC1H1 and SMN1 gene mutationsDian Kesumapramudya Nurputra, Jessica Sofian, Kristy Iskandar, et al.
F1000Research|November 27, 2023
Mutation spectrum analysis of <i>DMD</i> gene in Indonesian Duchenne and Becker muscular dystrophy patientsEry Kus Dwianingsih, Kristy Iskandar, Sunartini Hapsara, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|July 1, 2009
Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancyElisabeth Siti Herini, Gunadi, Marjan J A van Kempen, et al.
BMC Pediatrics|October 17, 2022
Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case reportKristy Iskandar, Sunartini, Farida Niken Astari, et al.
Plos One|October 31, 2022
Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophyKristy Iskandar, Agung Triono, Sunartini, et al.
Epilepsy Research|May 11, 2010
Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patientsElisabeth Siti Herini, Gunadi, Indra Sari Kusuma Harahap, et al.
BMC Research Notes|October 30, 2019
The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicineKristy Iskandar, Ery Kus Dwianingsih, Linda Pratiwi, et al.
International Journal of Neonatal Screening|October 19, 2020
Assessment of Spinal Muscular Atrophy Carrier Status by Determining <i>SMN1</i> Copy Number Using Dried Blood SpotsYogik Onky Silvana Wijaya, Jamiyan Purevsuren, Nur Imma Fatimah Harahap, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
BMC Proceedings|January 1, 2020
Use of air stacking to improve pulmonary function in Indonesian Duchenne muscular dystrophy patients: bridging the standard of care gap in low middle income country settingKristy Iskandar, Sunartini, Andika Priamas Nugrahanto, et al.
Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology|May 28, 2024
Multidisciplinary approach on divergent outcomes in spinal muscular atrophies: comparing DYNC1H1 and SMN1 gene mutationsDian Kesumapramudya Nurputra, Jessica Sofian, Kristy Iskandar, et al.
F1000Research|November 27, 2023
Mutation spectrum analysis of <i>DMD</i> gene in Indonesian Duchenne and Becker muscular dystrophy patientsEry Kus Dwianingsih, Kristy Iskandar, Sunartini Hapsara, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|July 1, 2009
Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancyElisabeth Siti Herini, Gunadi, Marjan J A van Kempen, et al.
BMC Pediatrics|October 17, 2022
Autosomal dominant Emery-Dreifuss muscular dystrophy caused by a mutation in the lamin A/C gene identified by exome sequencing: a case reportKristy Iskandar, Sunartini, Farida Niken Astari, et al.
Plos One|October 31, 2022
Dp71 and intellectual disability in Indonesian patients with Duchenne muscular dystrophyKristy Iskandar, Agung Triono, Sunartini, et al.
Epilepsy Research|May 11, 2010
Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patientsElisabeth Siti Herini, Gunadi, Indra Sari Kusuma Harahap, et al.
BMC Research Notes|October 30, 2019
The analysis of DMD gene deletions by multiplex PCR in Indonesian DMD/BMD patients: the era of personalized medicineKristy Iskandar, Ery Kus Dwianingsih, Linda Pratiwi, et al.
International Journal of Neonatal Screening|October 19, 2020
Assessment of Spinal Muscular Atrophy Carrier Status by Determining <i>SMN1</i> Copy Number Using Dried Blood SpotsYogik Onky Silvana Wijaya, Jamiyan Purevsuren, Nur Imma Fatimah Harahap, et al.
Pageof 2