Results 81 to 90 of about 38,461 (234)

‐adrenoceptor blockade and thyrotropin‐releasing hormone (TRH) on the cardiovascular system in the rabbit

, 1991
The effects of two different doses of thyrotropin-releasing hormone on regional blood flows were studied in urethane-anaesthetized rabbits pretreated with the alpha 2-adrenergic antagonists yohimbine and idazoxan.
L.‐O. D. KOSKINEN, Seligsohn, E. E., E. E. SELIGSOHN, Koskinen, Lars-Owe D.,   +3 more
core   +1 more source

Sex‐ and Region‐Specific Glial Reactivity in Hyperthyroid Mice Lacks Correlation With the Noncognitive and Non‐Depressive‐Like Behavioral Alterations

Brain and Behavior, Volume 16, Issue 6, June 2026.
Hyperthyroidism induces sex‐ and region‐specific glial reactivity without correlation to the noncognitive, non‐depressive behavioral changes in mice. ABSTRACT Background Glial reactivity is implicated in hyperthyroidism‐associated cognitive and psychiatric disorders, yet in vivo imaging evidence of glial reactivity in hyperthyroidism remains to be ...
Qianqian Xue, Zefang Lin, Yaofeng Wang, Xiuting Lin, Yun Yang, Chao Wang, Yuhong Ye, Weibing Miao   +7 more
wiley   +1 more source

Gonadotropin-Releasing Hormone in Milk [PDF]

, 1977
The hypothalamic hormone gonadotropin-releasing hormone (GnRH) has been found in milk of man, cow, and rat. Radioimmunoassays of acidified milk indicate concentrations of GnRH ranging between 0.1 and 3 nanograms per milliliter.
Koch, Yitzhak, Fridkin, Mati, Baram, Tallie, Hazum, Eli   +3 more
core   +1 more source

Thyrotropin-releasing hormone receptors in GtoPdb v.2023.1

, 2023
Thyrotropin-releasing hormone (TRH) receptors (provisional nomenclature as recommended by NC-IUPHAR [14]) are activated by the endogenous tripeptide TRH (pGlu-His-ProNH2). TRH and TRH analogues fail to distinguish TRH1 and TRH2 receptors [29].
Gershengorn, Marvin, Anthony P. Davenport, Rebecca Hills, Marvin Gershengorn, Davenport, Anthony P., Hills, Rebecca   +5 more
core   +1 more source

Neurocognitive Aging Following Acute Illness: Pathobiology and a Framework for Developing Neurotherapeutic Agents

Brain and Behavior, Volume 16, Issue 6, June 2026.
In this review, we discuss the scientific basis for how neurocognitive aging occurs after critical illness, including sepsis, trauma, and burns, and the clinical need to develop therapies to reduce inflammation, protect the blood–brain barrier, remove senescent cells, and enhance neuroplasticity.
Errin Lawrence, Daniel Fulton, Poppy Brown, Subashini Suresh, Mark Morris, Paraskevi Goggolidou, Sree Chaithanya, Marcus Abbawy, Amelia Wild, Prashant Nasa, Niharika A. Duggal, Fang Gao‐Smith, Zubair Ahmed, Suresh Renukappa, Tonny Veenith   +14 more
wiley   +1 more source

Primary Hypothyroidism With Markedly High Prolactin

Frontiers in Endocrinology, 2016
Secondary Pituitary enlargement due to primary hypothyroidism is not a common manifestation. The loss of thyroxin feedback inhibition in primary hypothyroidism causes overproduction of thyroid-releasing hormone (TRH), which results in secondary pituitary
MOHD SALEEM ANSARI, MUSSA H. ALMALKI, MUSSA H. ALMALKI   +2 more
doaj   +1 more source

Australian collaborative trial of antenatal thyrotropin-releasing hormone: adverse effects at 12-month follow-up

, 1997
Reports a 12-month follow up of the health and development of the children entered into the Australian Collaborative Trial of Antenatal Thyrotropin-Releasing Hormone (ACTOBAT).
Smith, D, HendersonSmart, D, Peres, M, Leslie, G, Ballesty, J, Arnold, J, Child, A, Crowther, C., Edwards, D, Haslam, R., Rowley, M, Nicholl, M, Reynolds, G, Robinson, J., Chin, M, Cook, C, Garvey, P, Gill, A, Evans, C, Walters, W, Downe, L, John, E, Likeman, R, Crowther, CA, Haslam, RR, Hiller, J., Hiller, JE, Fisher, C, Trudinger, B, Roberts, S, Chiltern, H, Giles, W, Robinson, JS, Ellwood, D, Pesce, A   +34 more
core   +1 more source

Hypokalemic Periodic Paralysis in a Young Woman With Mast Cell Activation Syndrome: A Case Report of an Atypical Presentation Associated With an Ultra‐Rare CACNA1S Variant

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Hypokalemic periodic paralysis (hKPP) is a rare neuromuscular channelopathy characterized by transient episodes of muscle weakness or paralysis associated with low serum potassium levels. It has been most commonly linked to autosomal dominant mutations in ion channel genes, specifically CACNA1S and SCN4A, which impair skeletal muscle ...
Ali Moradi, Yasmin Aboutaleb, Saba Noreen, Abdullah Sahyouni, Hasin Sharma, Olugbenga Oyesanmi, Ian M. Kahane, Yizhi Lin, Hakan R. Toka   +8 more
wiley   +1 more source

Homozygous TFR2 (c.2093_2096del) Mutation in an Asymptomatic Patient With Type 3 Hereditary Hemochromatosis, First Report From Saudi Arabia

Clinical Case Reports, Volume 14, Issue 6, June 2026.
ABSTRACT Hereditary hemochromatosis (HH) is an inherited disorder of iron metabolism characterized by progressive iron accumulation in multiple organs. While most cases are associated with HFE mutations, non‐HFE variants such as mutations in the transferrin receptor‐2 (TFR2) gene represent rare causes of iron overload.
Omar M. Raslan, Dana S. Alamoudi
wiley   +1 more source

The challenge of pituitary hyperplasia differential diagnosis in a young girl with growth arrest

Atti della Accademia Peloritana dei Pericolanti - Classe di Scienze Medico-Biologiche
Growth arrest is an alarming condition which requires precise and tempestive investigations in order to provide accurate diagnosis. Long-standing primary hypothyroidism (PHT) may rarely occur as a growth arrest as the only clinical sign at onset in ...
Aurora Lanzafame, Tiziana Abbate, Giuseppina Zirilli, Flavia Caime, Domenico Corica, Malgorzata Wasniewska   +5 more
doaj   +1 more source