Sunartini Hapsara
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View article: Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients
Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients Open
Background Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are allelic disorders caused by mutations in the DMD gene. The full mutation spectrum of the DMD gene in Indonesian patients is currently unknown. Mutation-sp…
View article: Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients
Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients Open
Background: Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are allelic disorders caused by mutations in the DMD gene. The full mutation spectrum of the DMD gene in Indonesian patients is currently unknown. Mutation-…
View article: Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients
Mutation spectrum analysis of DMD gene in Indonesian Duchenne and Becker muscular dystrophy patients Open
Background: Duchenne muscular dystrophy (DMD) and Becker muscular dystrophy (BMD) are allelic disorders caused by mutations in the DMD gene. The full mutation spectrum of the DMD gene in Indonesian patients is currently unknown. Mutation-…
View article: Incident Report: Between the Shadows of Obligation and Formality
Incident Report: Between the Shadows of Obligation and Formality Open
BACKGROUND: Incident reports are the primary data source for monitoring patient safety in the hospital. Monitoring of these reports determines the success of managing safety-related incidents as an effort to improve patient care. Hospital …
View article: Mutation Spectrum Analysis of DMD gene using MLPA method in Indonesian Duchenne and Becker muscular dystrophy patients
Mutation Spectrum Analysis of DMD gene using MLPA method in Indonesian Duchenne and Becker muscular dystrophy patients Open
Background: Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) are allelic disorders caused by mutations in DMD gene. The full mutation spectrum of DMD gene in Indonesian patients is currently unknown. Recently, mutation…
View article: Mutation Spectrum Analysis of DMD gene using MLPA method in Indonesian Duchenne and Becker muscular dystrophy patients
Mutation Spectrum Analysis of DMD gene using MLPA method in Indonesian Duchenne and Becker muscular dystrophy patients Open
Background: Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) are allelic disorders caused by mutations in DMD gene. The full mutation spectrum of DMD gene in Indonesian patients is currently unknown. Recently, mutation…
View article: Mutation Spectrum Analysis of DMD gene using MLPA method in Indonesian Duchenne and Becker muscular dystrophy patients
Mutation Spectrum Analysis of DMD gene using MLPA method in Indonesian Duchenne and Becker muscular dystrophy patients Open
Background: Duchenne Muscular Dystrophy (DMD) and Becker Muscular Dystrophy (BMD) are allelic disorders caused by mutations in DMD gene. The full mutation spectrum of DMD gene in Indonesian patients is currently unknown. Recently, mutation…
View article: Assessment of Spinal Muscular Atrophy Carrier Status by Determining SMN1 Copy Number Using Dried Blood Spots
Assessment of Spinal Muscular Atrophy Carrier Status by Determining SMN1 Copy Number Using Dried Blood Spots Open
Spinal muscular atrophy (SMA) is a common neuromuscular disease with autosomal recessive inheritance. The disease gene, SMN1, is homozygously deleted in 95% of SMA patients. Although SMA has been an incurable disease, treatment in infancy …
View article: Long-term follow up of a tuberous sclerosis patient: evaluation of anti-epileptic drugs and self- management support therapy
Long-term follow up of a tuberous sclerosis patient: evaluation of anti-epileptic drugs and self- management support therapy Open
Tuberous sclerosis (TSC) (OMIM 191100) is an inherited, autosomal dominant disorder affecting multiple organ systems.1 A genetic mutation in one of the tumor suppressor gene (TSG) alleles causes tumor growth in various organ systems. Tuber…
View article: Long-term follow up of a tuberous sclerosis patient: evaluation of anti-epileptic drugs and self- management support therapy
Long-term follow up of a tuberous sclerosis patient: evaluation of anti-epileptic drugs and self- management support therapy Open
Tuberous sclerosis (TSC) (OMIM 191100) is an inherited, autosomal dominant disorder affecting multiple organ systems.1 A genetic mutation in one of the tumor suppressor gene (TSG) alleles causes tumor growth in various organ systems. Tuber…
View article: THE INTERRATER RELIABILITY OF NURSING OUTCOME CLASSIFICATION (NOC): “SELF-CARE: EATING” ON MENTALLY DISABLED CHILDREN IN YOGYAKARTA
THE INTERRATER RELIABILITY OF NURSING OUTCOME CLASSIFICATION (NOC): “SELF-CARE: EATING” ON MENTALLY DISABLED CHILDREN IN YOGYAKARTA Open
Background: The common problems suffered by children with intellectual disability are difficulty to perform of daily activities or self-care including eating activity. NOC Self-care: eating is a measurement of client’s status regarding eat…
View article: Risk factors and the occurrence of cerebral palsy in high risk infants
Risk factors and the occurrence of cerebral palsy in high risk infants Open
Background The incidence of cerebral palsy (CP) has increased due to better survival rates of high-risk babies. Early detection and time to the occurrence of CP in the first year of life is important in order to provide early intervention.…
View article: Early detection of cerebral palsy in high-risk infants: diagnostic value of primitive and developmental reflexes as well as ultrasound
Early detection of cerebral palsy in high-risk infants: diagnostic value of primitive and developmental reflexes as well as ultrasound Open
Background The incidence of cerebral palsy (CP) has increased due to better survival of high-risk babies. A simple assessment method is needed for the early detection of CP, which can be performed by general practitioners and pediatricians…
View article: Early detection of cerebral palsy in high-risk infants: diagnostic value of primitive and developmental reflexes as well as ultrasound
Early detection of cerebral palsy in high-risk infants: diagnostic value of primitive and developmental reflexes as well as ultrasound Open
Background The incidence of cerebral palsy (CP) has increased due to better survival of high-risk babies. A simple assessment method is needed for the early detection of CP, which can be performed by general practitioners and pediatricians…
View article: The Readiness of Students to Learn Interprofessional Teamwork in Antenatal Care
The Readiness of Students to Learn Interprofessional Teamwork in Antenatal Care Open
Introduction: Indonesia as a developing country have a higher Maternal Mortality Rate (MMR). The prevention efforts is developing interprofessional collaborative practice (IPCP) in the level of health care. Collaboration attitudes should s…
View article: The Readiness of Students to Learn Interprofessional Teamwork in Antenatal Care
The Readiness of Students to Learn Interprofessional Teamwork in Antenatal Care Open
Introduction: Indonesia as a developing country have a higher Maternal Mortality Rate (MMR). The prevention efforts is developing interprofessional collaborative practice (IPCP) in the level of health care. Collaboration attitudes should s…