Acromegaly
What's New
Last Posted: Oct 02, 2024
- Correlation between insulin-like growth factor and complexity of glucose time series index in patients with newly diagnosed acromegaly: a PILOT study.
Lihua Zhou, et al. Endocrine 2024 0 - GH receptor polymorphisms guide second-line therapies to prevent acromegaly skeletal fragility: preliminary results of a pilot study.
Sabrina Chiloiro, et al. Frontiers in endocrinology 2024 0 1414101 - The Role of the GH Receptor Polymorphisms as a Prognostic Factor of Vertebral Fractures in Acromegalic Patients Resistant to First-generation SSAs and Treated with Pegvisomant or Pasireotide LAR.
Flavia Costanza, et al. Endocrine, metabolic & immune disorders drug targets 2024 0 - Germline AIP variants in sporadic young acromegaly and pituitary gigantism: clinical and genetic insights from a Han Chinese cohort.
Boni Xiang, et al. Endocrine 2024 0 - Pancreatic GHRHomas in Patients with or without Multiple Endocrine Neoplasia Type 1 (MEN 1) : An Analysis of 36 Reported Cases.
Ryuichi Yamasaki, et al. The journal of medical investigation : JMI 2024 0 (1.2) 1-8 - The spectrum of growth hormone excess in Carney complex and genotype-phenotype correlations.
Christina Tatsi, et al. The Journal of clinical endocrinology and metabolism 2024 0 - Genetic diagnosis in acromegaly and gigantism: From research to clinical practice.
Claudia Ramírez-Rentería et al. Best Pract Res Clin Endocrinol Metab 2024 101892 - Machine learning-based algorithms applied to drug prescriptions and other healthcare services in the Sicilian claims database to identify acromegaly as a model for the earlier diagnosis of rare diseases.
Salvatore Crisafulli et al. Sci Rep 2024 14(1) 6186 - FTO Gene Polymorphisms and Their Roles in Acromegaly.
Aleksandra Jawiarczyk-Przyby?owska, et al. International journal of molecular sciences 2023 0 (13) - Erectile function and androgen and estrogen beta receptor gene polymorphisms in acromegalic men.
F Pallotti, et al. Journal of endocrinological investigation 2023 0
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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
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- Graves Disease
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- 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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