Search Results

A retrospective cohort study evaluating pregnancy outcomes in women with MIDD.

• Authors : Sanchez-Lechuga, B.; Salvucci, M.; Ng, N.

Subjects: PREGNANCY outcomes; PREGNANCY; MISCARRIAGE

• Source: Acta Diabetologica; Mar2024, Vol. 61 Issue 3, p323-331, 9p

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Clinical Approaches for Mitochondrial Diseases.

• Authors : Hong, Seongho; Kim, Sanghun; Kim, Kyoungmi

Subjects: MITOCHONDRIAL DNA; MITOCHONDRIA; MITOCHONDRIAL proteins

• Source: Cells (2073-4409); Oct2023, Vol. 12 Issue 20, p2494, 25p

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Insulin Resistance in Mitochondrial Diabetes.

• Authors : Takano, Chika; Ogawa, Erika; Hayakawa, Satoshi

Subjects: TRANSFER RNA; INSULIN resistance; MITOCHONDRIAL DNA

• Source: Biomolecules (2218-273X); Jan2023, Vol. 13 Issue 1, p126, 12p

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The Mutations and Clinical Variability in Maternally Inherited Diabetes and Deafness: An Analysis of 161 Patients.

• Authors : Yang, Mengge; Xu, Lusi; Xu, Chunmei

Subjects: GENETIC mutation; CENTRAL nervous system diseases; CYTOPLASMIC inheritanceSPSS (Computer software)

• Source: Frontiers in Endocrinology; 11/25/2021, Vol. 12, p1-9, 9p

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Mitochondrial Bioenergetics and Dynamics in Secretion Processes.

• Authors : Martínez, Jennyfer; Marmisolle, Inés; Tarallo, Doménica

Subjects: BIOENERGETICS; SECRETION; IMMUNOGLOBULIN producing cells

• Source: Frontiers in Endocrinology; 5/22/2020, Vol. 11, p1-18, 18p

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Diabetes Mellitus in Mitochondrial Disease.

• Authors : Yi Shiau Ng; Taylor, Robert W.; Schaefer, Andrew M.

• Source: Frontiers in Diabetes; 2017, Vol. 25, p55-68, 14p

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m.3243A>G Mutation in Mitochondrial DNA Leads to Decreased Insulin Sensitivity in Skeletal Muscle and to Progressive γ-Cell Dysfunction.

• Authors : Lindroos, Markus M.; Majamaa, Kari; Tura, Andrea

Subjects: GENETIC mutation; MITOCHONDRIAL DNA; INSULIN

• Source: Diabetes; March2009, Vol. 58 Issue 3, p543-549, 7p, 2 Charts, 5 Graphs

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Clinical features, diagnosis and management of maternally inherited diabetes and deafness (MIDD) associated with the 3243A>G mitochondrial point mutation.

• Authors : Murphy, R.; Turnbull, D. M.; Walker, M.

Subjects: TYPE 2 diabetes; ENDOCRINE diseases; BLOOD plasma

• Source: Diabetic Medicine; Apr2008, Vol. 25 Issue 4, p383-399, 17p, 1 Color Photograph, 1 Diagram, 3 Charts

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Cowden disease: a review.

• Authors : Uppal, S.; Mistry, D.; Coatesworth, A. P.

• Source: International Journal of Clinical Practice; Apr2007, Vol. 61 Issue 4, p645-652, 8p

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β-Cell Function in Individuals Carrying the Mitochondrial tRNA Leu (UUR) Mutation.

• Authors : Salles, João Eduardo; Kasamatsu, Teresa S.; Dib, Sérgio A.

• Source: Pancreas; Jan2007, Vol. 34 Issue 1, p133-137, 5p

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