Results 121 to 130 of about 38,164 (259)

Risk factors for strangulating lipoma obstruction and lipomata in horses

open access: yesEquine Veterinary Journal, Volume 58, Issue 4, Page 1005-1015, July 2026.
Abstract Background Strangulating lipoma obstruction (SLO) is the most common cause of equine small intestinal strangulation and is fatal without surgery. Currently, epidemiological information is primarily limited to signalment‐related risk factors and requires further investigation.
Alex Gillen   +11 more
wiley   +1 more source

Is There a Genetic Link Between Resting Infrared Thermography in Young Horses and Longevity in Jumping Competition?

open access: yesJournal of Animal Breeding and Genetics, Volume 143, Issue 4, Page 481-495, July 2026.
ABSTRACT The objective was to evaluate the genetic relationship between the surface temperature of regions of interest, measured using infrared images of young horses and functional longevity in jumping. This relationship was assessed by comparing the temperatures measured in the offspring of two groups of sires, one favourable and one unfavourable, to
Anne Ricard   +3 more
wiley   +1 more source

ADRENOCORTICOTROPIC HORMONE IN HUMAN PLASMA* [PDF]

open access: yesJournal of Clinical Investigation, 1962
V K, VANCE   +3 more
openaire   +2 more sources

Glucocorticoid Receptor Translational Isoforms Generate Unique Glucocorticoid Responses in the Mouse Brain

open access: yesThe FASEB Journal, Volume 40, Issue 12, 30 June 2026.
GR‐A knockin mice were generated that express the classic full‐length glucocorticoid receptor (GR‐A) but lack the highly conserved translational isoforms GR‐B, GR‐C1, GR‐C2, GR‐C3, GR‐D1, GR‐D2, and GR‐D3 that have progressively shorter N‐terminal transactivation domains (NTDs).
Robert H. Oakley   +8 more
wiley   +1 more source

Metastatic esthesioneuroblastoma secreting adrenocorticotropic hormone in pediatric patients.

open access: yes, 2011
The purpose of this article was to report a pediatric case of secondary cervical esthesioneuroblastoma involving the parapharyngeal lymph nodes. A 3-year-old boy came to our clinical observation because of a right lymphonodal mass evidenced by nuclear ...
A. Arecchi   +7 more
core   +1 more source

Clinical Insights From a Case of Sifrim‐Hitz‐Weiss Syndrome With a CHD4 Variant: Expanding the Phenotypic Spectrum and Its Response to Growth Hormone Therapy

open access: yesAmerican Journal of Medical Genetics Part A, Volume 200, Issue 6, Page 1403-1410, June 2026.
ABSTRACT To enhance clinicians' understanding of Sifrim‐Hitz‐Weiss syndrome (SIHIWES), this study investigated the clinical phenotypes, genetic characteristics, and response to growth hormone therapy in a patient. A case of a patient with global developmental delay and distinctive facial features is presented.
Jianmei Zhang   +6 more
wiley   +1 more source

Hypopituarism - Not such an obvious symptom

open access: yesJournal of Education, Health and Sport
This paper presents the case of a diagnostic and therapeutic challenge of a young 33-year-old man from Poland, who initially reported few symptoms and eventually turned out to be an interesting endocrine case The pituitary gland is the central ...
Monika Grzybek   +9 more
doaj   +1 more source

Stress, stress systems, and Alzheimer's disease

open access: yesAlzheimer's &Dementia, Volume 22, Issue 6, June 2026.
Abstract Stress is increasingly recognized as an important, modifiable factor for Alzheimer's disease (AD), yet its roles in initiation, progression, and outcomes remain incompletely elucidated. Epidemiologic studies link chronic stress, early‐life adversity, and trauma to increased AD risk, while experimental models have uncovered mechanisms by which ...
Stephanie G. Eberly   +5 more
wiley   +1 more source

Two-dimensional NMR studies on 1-10 fragment of adrenocorticotropic hormone

open access: yes, 1992
Various two-dimensional NMR techniques have been used to obtain complete resonance assignments of the protons in the 1-10 fragment of adrenocorticotropic hormone (ACTH).
Tunga, A., Hosur, R. V.
core   +1 more source

Clinical Report and Genetic Analysis of a Patient With Congenital Hyperinsulinism Hyperammonemia Caused by a Novel Missense Mutation in the Structural Domain of the Isoform of the GLUD1 Gene

open access: yesClinical Case Reports, Volume 14, Issue 6, June 2026.
This patient was admitted to the hospital 43 h after birth with convulsions and hypoglycemia, presenting as recurrent refractory hypoglycemia that was difficult to control with conventional medication. Whole exome sequencing detected the GLUD1 (NM_005271.3:c.1495G>T, p.Gly499Cys) variant, which was a de novo variant in the patient and was not detected ...
Tingyu Li   +6 more
wiley   +1 more source

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