Results 211 to 220 of about 748,456 (359)

Practical Endocrinology

, 1936
Max A. Goldzieher
openalex   +1 more source

Society for Endocrinology: Officers [PDF]

, 1951

openalex   +1 more source

Heterozygous Med13l mice recapitulate a developmental growth delay and craniofacial anomalies seen in MED13L syndrome

Developmental Dynamics, EarlyView.
Abstract Background Gene transcription is crucial for embryo and postnatal development and is regulated by the Mediator complex. Mediator is comprised of four submodules, including the kinase submodule (CKM). The CKM consists of MED13, MED12, CDK8, and CCNC.
Anna K. Leinheiser, Timothy T. Nguyen, Kayla M. Henry, Mariela Rosales, Eric Van Otterloo, Chad E. Grueter   +5 more
wiley   +1 more source

Glycemic Analysis and Stratification of Pediatric Patients with Type 1 Diabetes Using isCGM in Southern Spain: Insights from the Andiacare Digital Platform. [PDF]

J Clin Med
Leiva-Gea I, Moreno-Jabato F, Ariza-Jiménez AB, Lendínez-Jurado A, Gómez-Perea A, Romero-Pérez MDM, García-García E, Santos Mata MÁ, Martínez-Moya G, Momblan J, Lechuga-Sancho AM, Gómez-Vida JM, Mier-Palacios M, Ranchal-Pérez MDP, Vivas-González G, Calleja Cabeza P, Fernández-Hernández E, Jiménez-Martín AP, Guarino-Narváez J, Rodríguez de Vera-Gómez P, Martínez-Brocca MA.   +20 more
europepmc   +1 more source

Clinical Endocrinology [PDF]

, 1954
Von Weidenbach W
openalex   +1 more source

Clinical Images: Methotrexate‐induced melanonychia

Arthritis &Rheumatology, EarlyView.
Yoshinori Taniguchi, Hirotaka Yamamoto
wiley   +1 more source

Pathogenesis and potential therapeutic targets of trichorhinophalangeal syndrome; lessons obtained from animal studies

Developmental Dynamics, EarlyView.
Abstract Trichorhinophalangeal syndrome (TRPS) is a rare genetic disease inherited in an autosomal dominant manner. It occurs in 1 in 100,000 people globally and is caused by several types of mutations of the TRPS1 gene. Since the first human patient was reported in 1966, typical and atypical pathologies, disease courses, and treatment case ...
Naoya Saeki, Rinna Kanai, Sayuri Tatsuta, Shinichi Kawaguchi, Masatsune Itoh, Shinsuke Ohba, Makoto Abe   +6 more
wiley   +1 more source

Ciba Foundation Colloquia on Endocrinology Vol. VII Synthesis and Metabolism of Adrenocortical Steroids [PDF]

, 1954

openalex   +1 more source

Parallel Increase in Childhood Anorexia Nervosa and Early Puberty During the COVID‐19 Pandemic

International Journal of Eating Disorders, EarlyView.
ABSTRACT Objective During the COVID‐19 pandemic, an increase in anorexia nervosa (AN), specifically childhood AN, as well as in central precocious puberty (CPP) and early‐onset puberty (EOP), was reported. The aim of this study was to explore whether there was a population‐level association between increases in both disorders and to discuss possible ...
Beate Herpertz‐Dahlmann, Astrid Dempfle, Stefan Eckardt, Josef Neulen, Kelly L. Klump   +4 more
wiley   +1 more source

When Severe Hypothyroidism Mimics Neuromuscular Diseases: A Case Supporting Outpatient Management in Contemporary Endocrinology. [PDF]

Cureus
Acanfora M, Presciuttini B, Benazzi D, Pulcina A, Pagani M.   +4 more
europepmc   +1 more source