Maternally Inherited Diabetes and Deafness (MIDD): Int'l Text of DM #157
Resolving complexity in mitochondrial disease: Towards precision medicine - ScienceDirect
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Mitochondrial diabetes and mitochondrial DNA mutation load in MELAS syndrome in: European Journal of Endocrinology Volume 183 Issue 5 (2020)
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Melas
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Genetische Erkrankungen und Diabetes mellitus - Endokrinologie & Diabetologie - Universimed - Medizin im Fokus
Mitochondrial diabetes and mitochondrial DNA mutation load in MELAS syndrome in: European Journal of Endocrinology Volume 183 Issue 5 (2020)
ArdorComm Media - Ayushman Bharat Block Health Melas conduct around 6 lakh diabetes screenings in a week - ArdorComm News Network https://ardorcomm-media.com/ayushman-bharat-block-health-melas -conduct-around-6-lakh-diabetes-screenings-in-a-week ...
Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes – a case report | BMC Neurology | Full Text
Diabetes and deafness - Wikipedia
PDF) Diagnosis of adult-onset MELAS syndrome in a 63-year-old patient with suspected recurrent strokes - A case report
MELAS Syndrome - Khondrion
MELAS AND OTHER MITOCHONDRIAL DISORDERS (Chapter 24) - Uncommon Causes of Stroke
A Juvenile Case of MELAS with T3271C Mitochondrial DNA Mutation | Pediatric Research
A Subtype of Diabetes Mellitus Associated with a Mutation of Mitochondrial DNA | NEJM
Over 6 lakh diabetes screenings in a week at Ayushman Bharat Block Health Melas : The Tribune India
TWO_FAMILIES_WITH_MIDD_AND_MELAS
Main causes of diabetes mellitus related to inborn errors of metabolism... | Download Table
David Melas - Member Board Of Directors - College of Logistics, Přerov | LinkedIn
Over 6 lakh diabetes screenings in a week at Ayushman Bharat Block Health Melas, ET HealthWorld
Reversing Mitochondrial Dysfunction is the Game Changer in Diabetes? - CME INDIA