• 20 Citations
  • 3 h-Index
20172019
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Fingerprint Dive into the research topics where Sara Al-Khawaga is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 1 Similar Profiles
Stem cells Chemical Compounds
Pluripotent Stem Cells Medicine & Life Sciences
Hypoglycemia Medicine & Life Sciences
Diabetes Mellitus Medicine & Life Sciences
Mutation Medicine & Life Sciences
Medical problems Chemical Compounds
Lafora Disease Medicine & Life Sciences
Congenital Hyperinsulinism Medicine & Life Sciences

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Research Output 2017 2019

  • 20 Citations
  • 3 h-Index
  • 7 Article
  • 1 Comment/debate
  • 1 Review article

A SLC16A1 mutation in an infant with ketoacidosis and neuroimaging assessment: Expanding the clinical spectrum of MCT1 deficiency

Al-Khawaga, S., AlRayahi, J., Khan, F., Saraswathi, S., Hasnah, R., Haris, B., Mohammed, I., Mohamed, E. & Hussain, K., 1 Jul 2019, In : Frontiers in Pediatrics. 7, JULY, 299.

Research output: Contribution to journalArticle

Open Access
Ketosis
Neuroimaging
Mutation
Lactic Acid
Genes
1 Citation (Scopus)

Diabetes mellitus in a patient with lafora disease: Possible links with pancreatic β-cell dysfunction and insulin resistance

Nicolescu, R. C., Al-Khawaga, S., Minassian, B. A. & Hussain, K., 1 Jan 2019, In : Frontiers in Pediatrics. 6, JAN, 424.

Research output: Contribution to journalArticle

Open Access
Lafora Disease
Glycogen
Insulin Resistance
Diabetes Mellitus
Mutation

Ion transporters, channelopathies, and glucose disorders

Demirbilek, H., Galcheva, S., Vuralli, D., Al-Khawaga, S. & Hussain, K., 2 May 2019, In : International journal of molecular sciences. 20, 10, 2590.

Research output: Contribution to journalReview article

Open Access
Channelopathies
diabetes mellitus
transporter
Facilitative Glucose Transport Proteins
Medical problems

The clinical and genetic characteristics of permanent neonatal diabetes (PNDM) in the state of Qatar

Al-Khawaga, S., Mohammed, I., Saraswathi, S., Haris, B., Hasnah, R., Saeed, A., Almabrazi, H., Syed, N., Jithesh, P. V., El Awwa, A., Khalifa, A., AlKhalaf, F., Petrovski, G., Mohamed, E. & Hussain, K., 1 Jan 2019, In : Molecular Genetics and Genomic Medicine. e753.

Research output: Contribution to journalArticle

Open Access
Qatar
Diabetes Mellitus
Live Birth
Mutation
Pancreas

The genetic and molecular mechanisms of congenital hyperinsulinism

Galcheva, S., Demirbilek, H., Al-Khawaga, S. & Hussain, K., 1 Jan 2019, In : Frontiers in Endocrinology. 10, FEB, 111.

Research output: Contribution to journalArticle

Open Access
Congenital Hyperinsulinism
Molecular Biology
Hypoglycemia
Insulin
Hepatocyte Nuclear Factor 1