Zobrazeno 1 - 10
of 144
pro vyhledávání: '"Saraswati, A"'
Autor:
Uzma Shamim, Seena Vengalil, Kiran Polavarapu, Atchayaram Nalini, Sanita Raju, Hanns Lochmüller, Dhaarini Mohan, Shingavi Leena, Aradhana Mathur, Saraswati Nashi, Tanushree Chawla, Mohammed Faruq, Aditi Joshi, Sushmita Nayak, Chandrajit Prasad, Veeramani Preethish-Kumar, Mainak Bardhan, Shahyan Siddiqui
Publikováno v:
Journal of Neuromuscular Diseases. 9:95-109
Background and Purpose: Mutations in the GMPPB gene affect glycosylation of α-dystroglycan, leading to varied clinical phenotypes. We attempted to delineate the muscle MR imaging spectrum of GMPPB-related Congenital Myasthenic syndrome (CMS) in a si
Publikováno v:
Indian Journal of Forensic and Community Medicine. 8:166-169
Background: The growth and development of child is a strong reflection of country's growth and development. Being most vulnerable segment of the society the preschoolers are at greatest risk of malnutrition for it is their growing period that demands
Autor:
Dinesh Reghunathan, Veeramani Preethish-Kumar, Nalini Atchayaram, Muhammed Faruq, Sima Chaudhari, Kiran Polavarapu, Gayathri Narayanappa, Aditi Joshi, Rashmi Santhoshkumar, Kapaettu Satyamoorthy, Seena Vengalil, Saraswati Nashi
Publikováno v:
Journal of Molecular Neuroscience. 71:2468-2473
Desminopathies (MIM*601419) are clinically heterogeneous, manifesting with myopathy and/or cardiomyopathy and with intra-sarcoplasmic desmin-positive deposits. They have either an autosomal dominant (AD) or recessive (AR) pattern of inheritance. Desm
Publikováno v:
Journal of Complementary and Integrative Medicine. 19:571-579
Objectives Alcohol consumption causes several harmful effects on the organs, which is hugely understated. Many deformities occur in the fetus when pregnant mothers indulge in alcoholism. Alcohol is a known teratogen, hence organ formation, particular
Autor:
Veeramani Preethish-Kumar, Atchayaram Nalini, Rita Horvath, Nandeesh Bevinahalli, Ram Murthy Anjanappa, Saraswati Nashi, Mainak Bardhan, Seena Vengalil, Ichizo Nishino, Gautham Arunachal, Divya Nagabushana, Tanushree Chawla, Dhaarini Mohan, Kiran Polavarapu, Leena Shingavi
Publikováno v:
Journal of Human Genetics. 66:813-823
Megaconial congenital muscular dystrophy (CMD)(OMIM #602541), related to CHKB mutation, is a rare autosomal recessive disorder. To date, only 35 confirmed patients are recorded. We present a detailed description of the clinical, histopathological, im
Publikováno v:
BMC Psychiatry, Vol 21, Iss 1, Pp 1-11 (2021)
BMC Psychiatry
BMC Psychiatry
Background Quality of life is an important indicator of health and has multiple dimensions. It is adversely affected in patients with trauma history, and psychiatric disorders play an important role therein. Studies in trauma-affected populations foc
Publikováno v:
International Journal of Pharma Medicine and Biological Sciences. 10:35-39
Autor:
Putu Ayu Parwati, Niken Ayu Merna Eka Sari, Ni Luh Gede Intan Saraswati, Ni Komang Ayu Resiyanthi, I Gusti Ayu Putu Satya Laksmi
Publikováno v:
jurnalempathy.com. 1:165-171
Background: PHBS at school age that is not good enough will cause various diseases such as diarrhea, toothache, skin pain and worms. Thus, to reduce the prevalence of these bad impacts, it is important to apply PHBS. Methods: The method used is the l
Publikováno v:
JURNAL KESEHATAN STIKes MUHAMMADIYAH CIAMIS. 7:34-48
Thalasemia atau disebut anemia mediterania adalah penyakit keturunan yang terjadi akibat kurangnya jumlah sel darah merah di dalam tubuh manusia sehingga produksi hemoglobin menjadi berkurang. Berdasarkan data dari ruang thalassemia RSUD Kabupaten Ci
ANALISIS METODE PENGOLAHAN DATA KASUS OUTAGE TRANSMISI SERAT OPTIK: STUDI KASUS JARINGAN TIGA REGION
Publikováno v:
Jurnal Elektro. 13:39-50
The wide implementation of fibre optic transmission cable supports the increasing demand of datacommunication, due to its reliability and its fast connectivity. However, optical fibre communicationmight experience an outage condition, which could deg