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Inherited Diabetes sentence examples within mitochondrial encephalomyopathy lactic



One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation


Concomitant Mitochondrial Diabetes and Myopathy Mistook for Complications of Immunosuppressants After Kidney Transplant.

Inherited Diabetes sentence examples within mitochondrial encephalopathy lactic



The Spectrum of Maculopathy in Mitochondrial DNA A3243G Mutation: A Case Series of Six Patients.


Sensitive quantification of m.3243A>G mutational proportion in non-retinal tissues and its relationship with visual symptoms.

Inherited Diabetes sentence examples within Maternally Inherited Diabetes



Mitochondrial Diabetes: The Clinical Spectrum of MIDD and MELAS in Association With the A3243G Mutation


One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation


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Inherited Diabetes sentence examples within inherited diabetes mellitu



SUN-LB033 New Onset Diabetes in a Post-Renal Transplant Pediatric Patient with a Mutation of the Hepatocyte Nuclear Factor-1β Gene


SUN-130 A Not-So-Simple Work-Up of Diabetes: A Case of MODY 5


Mitochondrial Diabetes: The Clinical Spectrum of MIDD and MELAS in Association With the A3243G Mutation



One mutation, three phenotypes: novel metabolic insights on MELAS, MIDD and myopathy caused by the m.3243A > G mutation



Gene Panel Sequencing of Patients With Monogenic Diabetes Brings to Light Genes Typically Associated With Syndromic Presentations.



Sleep-Disordered Breathing in Adult Patients With Mitochondrial Diseases



Chronic intestinal psuedo-obstruction and MIDD, a rare cause of acute abdomen: implications in emergency surgery



Etiologic distribution and clinical characteristics of pediatric diabetes in 276 children and adolescents with diabetes at a single academic center



Concomitant Mitochondrial Diabetes and Myopathy Mistook for Complications of Immunosuppressants After Kidney Transplant.



Glucagon-like peptide-1 receptor agonists (GLP1-RA) in the treatment of mitochondrial diabetes



Authors’ reply to “m.3243A>G carriers develop syndromic or non-syndromic multisystem phenotypes over time”



Multimodal imaging analysis of macular dystrophy in patient with maternally inherited diabetes and deafness (MIDD) with m.3243A>G mutation



Mitochondrial Retinopathy.



The Spectrum of Maculopathy in Mitochondrial DNA A3243G Mutation: A Case Series of Six Patients.



The Role of Mitochondrial Mutations and Chronic Inflammation in Diabetes



Mutational Analysis of Mitochondrial tRNA Genes in 200 Patients with Type 2 Diabetes Mellitus



Maternally inherited diabetes and deafness coexists with lipoprotein lipase gene mutation associated severe hyperlipidemia that was resistant to fenofibrate and atorvastatin but sensitive to bezafibrate: a case report.



Sensitive quantification of m.3243A>G mutational proportion in non-retinal tissues and its relationship with visual symptoms.



Maternally inherited diabetes and deafness (MIDD): An uncommon but important cause of diabetes



Treating hypercholesterinemia in a patient with maternally inherited diabetes and deafness (MIDD) by the proprotein convertase subtilisin/kexin type 9 (PCSK9) inhibitor alirocumab



Monogenic Diabetes: Genetics and Relevance on Diabetes Mellitus Personalized Medicine.



MON-122 Familial Clinical Heterogeneity Manifested by the Presence of Either Diabetes or Deafness in a Pedigree of a Patient with Maternally Inherited Diabetes Mellitus and Deafness and Mitochondrial DNA M.3243a>G Mutation



SUN-LB033 New Onset Diabetes in a Post-Renal Transplant Pediatric Patient with a Mutation of the Hepatocyte Nuclear Factor-1β Gene



SUN-130 A Not-So-Simple Work-Up of Diabetes: A Case of MODY 5



mTOR inhibitors may benefit kidney transplant recipients with mitochondrial diseases.



THE ROLE OF HETEROPLASMY IN THE DIAGNOSIS AND MANAGEMENT OF MATERNALLY INHERITED DIABETES AND DEAFNESS.



Dynamic derangement in amino acid profile during and after a stroke-like episode in adult-onset mitochondrial disease: a case report



Quantitative Variation in m.3243A > G Mutation Produce Discrete Changes in Energy Metabolism



De Novo Mutation of m.3243A>G together with m.16093T>C Associated with Atypical Clinical Features in a Pedigree with MIDD Syndrome



Audiological and Vestibular Findings in Subjects with MELAS Syndrome.



Progression of Peripheral Vestibular Dysfunctions in Patients With a Mitochondrial A3243G Mutation.


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Inherited Diabetes 유전성 당뇨병


Inherited Diabetes 유전성 당뇨병
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