Results 11 to 20 of about 48,699 (150)

The TRH test provides valuable information in the diagnosis of central hypothyroidism in patients with known pituitary disease and low T4 levels [PDF]

open access: yesFrontiers in Endocrinology, 2023
ObjectiveTo evaluate the value of the thyrotropin-releasing hormone (TRH) test in the diagnosis of central hypothyroidism (CH) in patients with pituitary disease.MethodsSystematic evaluation of 359 TRH tests in patients with pituitary disease including ...
Sara Ellegaard Christensen   +10 more
doaj   +2 more sources

Succinic semialdehyde dehydrogenase deficiency presenting with central hypothyroidism [PDF]

open access: yesClinical Case Reports, 2021
Central hypothyroidism might be another clinical sign of SSADH deficiency which prompts urinary organic acid screening for GHB in central hypothyroidism patients. Studies on GABA and thyroid hormone interaction might be a concept of a new therapy.
Malak Ali Alghamdi   +6 more
doaj   +2 more sources

Central hypothyroidism or subclinical hyperthyroidism: can they be confused with each other? [PDF]

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2020
Isolated, adult-onset central hypothyroidism is very rare, and its diagnosis can be challenging. A 42-year-old patient was referred for evaluation of a 2.8 cm thyroid nodule.
Mauro Boronat
doaj   +2 more sources

Novel TSHB variant (c.217A>C) causing severe central hypothyroidism and pituitary hyperplasia [PDF]

open access: yesEndocrinology, Diabetes & Metabolism Case Reports, 2022
Biallelic pathological variants in the thyroid stimulating hormone (TSH) subunit β gene (TSHB) result in isolated TSH deficiency and secondary hypothyroidism, a rare form of central congenital hypothyroidism (CCH), with an estimated incidence of 1 in 65 ...
Adam I Kaplan   +2 more
doaj   +2 more sources

Immediate postnatal central hypothyroidism caused by maternal Graves' disease: Importance of early screening [PDF]

open access: yesClinical Case Reports, 2022
This report illustrates a case of central hypothyroidism in a newborn immediately after birth caused by maternal Graves' disease. Infants from mothers with Graves' disease require careful examination without waiting for neonatal screening results, even ...
Saho Tochibora   +9 more
doaj   +2 more sources

Low cholesterol levels are good markers for central hypothyroidism in case with dialysis using roxadustat [PDF]

open access: yesClinical Case Reports
Key Clinical Message Recently, hypoxia‐inducible factor prolyl hydroxylase (HIF‐PH) inhibitors have been used for renal anemia, but side effects have also been reported.
Serina Kita   +9 more
doaj   +2 more sources

Practical and pragmatic usage of T3 in hypothyroidism

open access: yesIndian Journal of Endocrinology and Metabolism, 2023
Hypothyroidism is one of the common endocrine disorders encountered in clinical practice. Though thyroxine (T4) remains the treatment of choice in most clinical situations, with the recent introduction of oral triiodothyronine (T3) in South Asian ...
Sanjay Kalra   +3 more
doaj   +1 more source

Case report: Central-pituitary hypothyroidism concurrent with hyperadrenocorticism without pituitary macroadenoma in a Miniature Schnauzer dog

open access: yesFrontiers in Veterinary Science, 2023
Multiple endocrine disorders are uncommon in veterinary medicine, and the disease combination is usually related to hypercortisolism or autoimmunity.
Yeon Chae   +6 more
doaj   +1 more source

A Case of Congenital Central Hypothyroidism Caused by a Novel Variant (Gln1255Ter) in IGSF1 Gene

open access: yesJCRPE, 2021
Loss-of-function mutations in the immunoglobulin superfamily, member 1 (IGSF1) gene cause X-linked central hypothyroidism, and therefore its mutation affects mainly males.
Doğa Türkkahraman   +2 more
doaj   +1 more source

GH Deficiency and Replacement Therapy in Hypopituitarism: Insight Into the Relationships With Other Hypothalamic-Pituitary Axes

open access: yesFrontiers in Endocrinology, 2021
GH deficiency (GHD) in adult patients is a complex condition, mainly due to organic lesion of hypothalamic-pituitary region and often associated with multiple pituitary hormone deficiencies (MPHD).
Eriselda Profka   +5 more
doaj   +1 more source

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