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All Journal Jurnal Keperawatan Jiwa (JKJ): Persatuan Perawat Nasional Indonesia Jurnal Kedokteran dan Kesehatan : Publikasi Ilmiah Fakultas Kedokteran Universitas Sriwijaya Biomedical Journal of Indonesia Indonesian Journal for Health Sciences (IJHS) SRIWIJAYA JOURNAL OF MEDICINE Bioscientia Medicina : Journal of Biomedicine and Translational Research Scientia Psychiatrica Jurnal Psikiatri Surabaya (Surabaya Psychiatry Journal) Archives of The Medicine and Case Reports Bioscientia Medicina : Journal of Biomedicine and Translational Research International Journal of Islamic and Complementary Medicine
Bintang Arroyantri Prananjaya
Departemen Ilmu Kedokteran Jiwa, Fakultas Kedokteran, Universitas Sriwijaya
Religion Biochemistry, Genetics & Molecular Biology Education Health Professions Immunology & microbiology Medicine & Pharmacology Neuroscience Nursing Physics Public Health Veterinary

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GENETICS OF DEMENTIA: THE CANDIDATE GENES AND AVAILABLE GENETIC TESTINGS Ziske Maritska; Diah Andini; Febryana Ramadhani Machyar; Rachmat Taufan; Try Merdeka Puri; Tryvanie R Putra; Uswati Uswati; Bintang Arroyantri Prananjaya; Rini Nindela; Nita Parisa
Indonesian Journal for Health Sciences Vol 7, No 2 (2023): September
Publisher : Universitas Muhammadiyah Ponorogo

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.24269/ijhs.v7i2.6353

Abstract

When dementia is present, a person's memory, reasoning, behavior, and even their capacity to carry out day-to-day chores can all become distorted. This syndrome remains present and actually worsens as time passes. It's possible that synapse loss, death and dysfunction of brain cells, gliosis, and inflammation are all factors in the progression of dementia. The clinical syndrome, age, and a history of the ailment in the patient's family should dictate the choices made about counseling and testing. Dementia is known as a multifactorial condition, brought on by the combination of strong genetic factors and environmental factors. There are several candidate genes  associated with Dementia; APP, PSEN1, and PSEN2 genes, in addition to the GRN and MAPT genes. This literatura review provide insight on the genetic of Dementia, particularly in the genetic causes and testings
Neuropsychiatric Aspects of Long Covid Bintang Arroyantri Prananjaya; Muhammad Yusuf Wijahaska; Chris Alberto Amin; Carissa Delania; Ziske Maritska; Nita Parisa; Mohammad Hilal Atthariq Ramadhan
Biomedical Journal of Indonesia Vol. 8 No. 1 (2022): Vol 8, No 1, 2022
Publisher : Fakultas Kedokteran Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.32539/BJI.v8i1.125

Abstract

Long COVID is a term used for persistent symptoms after being infected with COVID-19 with an estimated point of onset ranging from 3-12 weeks after infection. The risk factors for the occurrence of Long COVID are influenced by age, gender, comorbidity, ethnicity, and the severity of the acute phase. It is known that central, peripheral, and psychological factors play an important role in chronic fatigue, which is one of the most common symptoms of Long COVID. The most common neuropsychiatric clinical manifestations in Long COVID are sleep disturbances, fatigue, depression, anxiety disorders, decreased cognitive function or decreased concentration, and post-traumatic stress disorder. Therapeutic management for Long COVID cases involves various aspects, such as physical rehabilitation, management of pre-existing co-morbidities, mental health support management, and social services.
SARCOPENIA IN ELDERLY PATIENTS: WHAT ARE THE CONTRIBUTING RISK FACTORS? Muhammad Raihan Afif Kurniawan; Nur Riviati; Bintang Arroyantri Prananjaya; Muhammad Reagan; Syarifah Aini
Jurnal Kedokteran dan Kesehatan : Publikasi Ilmiah Fakultas Kedokteran Universitas Sriwijaya Vol. 11 No. 2 (2024): Jurnal Kedokteran dan Kesehatan : Publikasi Ilmiah Fakultas Kedokteran Univers
Publisher : Fakultas Kedokteran Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.32539/jkk.v11i2.389

Abstract

Sarcopenia in Elderly Patients: What are the Contributing Risk Factors?. Sarcopenia is the gradual loss of muscle mass associated with aging. The process by which sarcopenia occurs is not fully understood. Many factors are at risk of causing sarcopenia, such as age, gender, and physical activity. Early detection with the SARC-F questionnaire is needed to prevent sarcopenia. This study is a descriptive observational study with a cross-sectional approach with total sampling to see the description of sarcopenia and risk factors in elderly patients at the Geriatric Polyclinic of Dr. Mohammad Hoesin Hospital Palembang. Primary data were collected through interviews using a questionnaire, and then analyzed univariately. A total of 48.4% of the elderly at the Geriatric Polyclinic of Dr. Mohammad Hoesin Hospital Palembang had sarcopenia findings. Patients in the sarcopenia group were mostly aged 70-79 years (41.9%), female (64.5%), married (58.1%), history of primary education (32.3%), had worked (58.1%), had mild comorbidities (58.1%), sedentary physical activity (74.2%), and at risk of malnutrition (54.8%).
Genetic Factors Affecting Neuroplasticity Ziske Maritska; Muhammad Fakhri Altyan; Ardy Oktaviandi; Muhammad Barkah; Amirah Dhia Nabila Sinum; Emelda Emelda; Hawari Martanusa; Rini Nindela; Nita Parisa; Bintang Arroyantri Prananjaya; Puji Rizki Suryani; Eka Febri Zulissetiana
Sriwijaya Journal of Medicine Vol. 6 No. 2 (2023): Vol 6, No. 2, 2023
Publisher : Fakultas Kedokteran Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.32539/sjm.v6i2.152

Abstract

Neuroplasticity pertains to the brain's ability to adjust functions or structure in response to events and is an important factor for skill-learning development as well as functional recovery from a neurological disorder. Numerous factors could influence neuroplasticity processes. This literature review aims to discuss the roles of genetic factors in neuroplasticity. The literature search was conducted using the keywords “neuroplasticity”, genetics”, “genes”, and polymorphism” in search engines like google scholar and PubMed, covering original articles, reviews, and text book both in Bahasa Indonesia and English for the last ten years. Genetic variation including gene polymorphism was responsible for the impact of BDNF, ApoE, and dopamine on the functional neural repair of the brain. Certain processes might directly influence neuroplasticity; others might interfere indirectly through the process. A deeper insight into genetic influence regarding neuroplasticity could lead to a better understanding and potential improvement of treatment.
Genetic Conditions Associated with Intellectual Disability in Indonesian Population: A Review Ziske Maritska; Atikah M. Ihsan; Ina Rahmawati; Perawati Perawati; Mohammad Hilal Atthariq Ramadhan; Bintang Arroyantri Prananjaya; Nita Parisa
Sriwijaya Journal of Medicine Vol. 7 No. 1 (2024): Vol 7, No 1, 2024
Publisher : Fakultas Kedokteran Universitas Sriwijaya

Show Abstract | Download Original | Original Source | Check in Google Scholar | DOI: 10.32539/sjm.v7i1.220

Abstract

Intellectual disability (ID) brings challenges to the affected individuals, their families, and the community at large. It is a multifactorial condition with many contributing factors, namely genetics. This review aims to briefly provide several related genetic conditions for ID in the Indonesian population. Literature studies search relevant articles using PubMed and Google Scholar using the terms ‘intellectual disability’, ‘genetics', ‘Indonesian population’. In Indonesia, the prevalence of children with ID is 1–3%, with 62,011 school-aged children affected with Intellectual Disability. Genetics plays a role in around 25–50% of cases. ID in the Indonesian population is associated with several genetic disorders, namely Duchenne muscular dystrophy (DMD), autism spectrum disorder (ASD), fragile X syndrome (FXS), Down syndrome (DS), Apert syndrome, and subtelomeric chromosomal rearrangements. There is limited research on genetics related to intellectual disability in Indonesia, implying further research is needed.
Co-Authors Alessandro Syafei Rashid Alfadea Irbah Allizaputri Amirah Dhia Nabila Sinum Andhika Diaz Maulana Ardesy Melizah Kurniati Ardy Oktaviandi Atikah M. Ihsan Carissa Delania Chandra Wahyudi Chris Alberto Amin Diah Andini Diyaz Syauki Ikhsan Eka Febri Zulissetiana Emelda Emelda Febryana Ramadhani Machyar Hawari Martanusa Ina Rahmawati Indri Seta Septadina Jiann Lin Loo Kaima Ishmata Rianti M. Khairul Kahfi Pasaribu Mohammad Hilal Atthariq Ramadhan Muhammad Barkah Muhammad Fakhri Altyan Muhammad Hilal Atthariq Ramadhan Muhammad Raihan Afif Kurniawan Muhammad Reagan Muhammad Yusuf Wijahaska Nita Parisa Nur Riviati Perawati Perawati Puji Rizki Suryani Puji Rizki Suryani Rachmat Taufan Rahmi Isman Rini Nindela Rini Nindela Rovania Yantinez Quardetta Syarifah Aini Try Merdeka Puri Tryvanie R Putra Uswati Uswati Ziske Maritska