Permanent Neonatal Diabetes Mellitus
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Last Posted: May 04, 2024
- Computational Analysis of Deleterious nsSNPs in INS Gene Associated with Permanent Neonatal Diabetes Mellitus.
Elsadig Mohamed Ahmed, et al. Journal of personalized medicine 2024 0 (4) - [Clinical and genetic analysis of an infant with permanent neonatal diabetes mellitus due to novel variant of insulin gene].
Li Mali, et al. Zhonghua yi xue yi chuan xue za zhi = Zhonghua yixue yichuanxue zazhi = Chinese journal of medical genetics 2022 0 (1) 66-70 - Genetic and clinical heterogeneity of permanent neonatal diabetes mellitus: a single tertiary centre experience.
Laimon Wafaa, et al. Acta diabetologica 2021 0 (12) 1689-1700 - Insulin gene mutations linked to permanent neonatal diabetes mellitus in Indian population.
Gopi Sundaramoorthy, et al. Journal of diabetes and its complications 2021 0 (12) 108022 - Identification of insulin gene variants in patients with neonatal diabetes in the Chinese population.
Fu Junling, et al. Journal of diabetes investigation 2019 10 - Monogenic Forms of Diabetes Mellitus.
Gaál Zsolt et al. Experientia supplementum (2012) 2019 111385-416 - A Genotype-First Approach for Clinical and Genetic Evaluation of Wolcott-Rallison Syndrome in a Large Cohort of Iranian Patients with Neonatal Diabetes.
Abbasi Farzaneh et al. Canadian journal of diabetes 2017 Aug - Phenotypic heterogeneity in monogenic diabetes: the clinical and diagnostic utility of a gene panel-based next-generation sequencing approach.
Alkorta-Aranburu G, et al. Molecular genetics and metabolism 2014 12 (4) 315-20 - Amino acid properties may be useful in predicting clinical outcome in patients with Kir6.2 neonatal diabetes.
Fraser Clementine S, et al. European journal of endocrinology / European Federation of Endocrine Societies 2012 9 (3) 417-21 - Permanent neonatal diabetes mellitus
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Selected Rare Diseases
- Alpha-1 Antitrypsin Deficiency
- Amyotrophic Lateral Sclerosis
- Brugada Syndrome
- Cerebral Palsy
- Cystic Fibrosis
- Duchenne Muscular Dystrophy
- Eclampsia
- Erythema Multiforme
- Familial Mediterranean Fever
- Fragile X Syndrome
- Gaucher Disease
- Glomerulonephritis
- Graves Disease
- Hemophilia
- Huntington Disease
- Microcephaly
- Myasthenia Gravis
- Phenylketonuria
- Retinitis Pigmentosa
- Severe Combined Immunodeficiency
Disclaimer: Articles listed in the Public Health Knowledge Base are selected by Public Health Genomics Branch to provide current awareness of the literature and news. Inclusion in the update does not necessarily represent the views of the Centers for Disease Control and Prevention nor does it imply endorsement of the article's methods or findings. CDC and DHHS assume no responsibility for the factual accuracy of the items presented. The selection, omission, or content of items does not imply any endorsement or other position taken by CDC or DHHS. Opinion, findings and conclusions expressed by the original authors of items included in the update, or persons quoted therein, are strictly their own and are in no way meant to represent the opinion or views of CDC or DHHS. References to publications, news sources, and non-CDC Websites are provided solely for informational purposes and do not imply endorsement by CDC or DHHS.
- Page last reviewed:Feb 1, 2024
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