Biomaterial Database

[Excretion of 17-ketosteroids in various endocrine diseases]. 1963

A S GRINSHPUN

UI	MeSH Term	Description	Entries
D006980	Hyperthyroidism	Hypersecretion of THYROID HORMONES from the THYROID GLAND. Elevated levels of thyroid hormones increase BASAL METABOLIC RATE.	Hyperthyroid,Primary Hyperthyroidism,Hyperthyroidism, Primary,Hyperthyroids
D003480	Cushing Syndrome	A condition caused by prolonged exposure to excess levels of cortisol (HYDROCORTISONE) or other GLUCOCORTICOIDS from endogenous or exogenous sources. It is characterized by upper body OBESITY; OSTEOPOROSIS; HYPERTENSION; DIABETES MELLITUS; HIRSUTISM; AMENORRHEA; and excess body fluid. Endogenous Cushing syndrome or spontaneous hypercortisolism is divided into two groups, those due to an excess of ADRENOCORTICOTROPIN and those that are ACTH-independent.	Cushing's Syndrome,Hypercortisolism,Syndrome, Cushing,Syndrome, Cushing's
D004700	Endocrine System Diseases	Pathological processes of the ENDOCRINE GLANDS, and diseases resulting from abnormal level of available HORMONES.	Endocrine Diseases,Diseases of Endocrine System,Disease, Endocrine,Disease, Endocrine System,Diseases, Endocrine,Diseases, Endocrine System,Endocrine Disease,Endocrine System Disease,System Disease, Endocrine,System Diseases, Endocrine
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000075262	Hypoadrenocorticism, Familial	Hereditary forms of Addison disease that may exhibit autosomal recessive or X-linked inheritance. They are characterized by severe neurological symptoms, APNEA; and death in infancy. OMIM: 240200	AHC with Isolated Gonadotropin Deficiency,Addison Disease, X-Linked,Adrenal Hypoplasia, Congenital,Adrenal Hypoplasia, Congenital, with Hypogonadotropic Hypogonadism,Complex Glycerol Kinase Deficiency,Cytomegalic Adrenocortical Hypoplasia,Familial X-linked Addison Disease,X-linked Adrenal Hypoplasia,X-linked Congenital Adrenal Hypoplasia,Xp21 Contiguous Gene Deletion Syndrome,Addison Disease, X Linked,Adrenal Hypoplasia, X-linked,Congenital Adrenal Hypoplasia,Congenital Adrenal Hypoplasias,Cytomegalic Adrenocortical Hypoplasias,Familial Hypoadrenocorticism,Familial Hypoadrenocorticisms,Familial X linked Addison Disease,Hypoadrenocorticisms, Familial,Hypoplasia, Congenital Adrenal,X linked Adrenal Hypoplasia,X linked Congenital Adrenal Hypoplasia,X-Linked Addison Disease
D000172	Acromegaly	A condition caused by prolonged exposure to excessive HUMAN GROWTH HORMONE in adults. It is characterized by bony enlargement of the FACE; lower jaw (PROGNATHISM); hands; FEET; HEAD; and THORAX. The most common etiology is a GROWTH HORMONE-SECRETING PITUITARY ADENOMA. (From Joynt, Clinical Neurology, 1992, Ch36, pp79-80)	Inappropriate Growth Hormone Secretion Syndrome (Acromegaly),Somatotropin Hypersecretion Syndrome (Acromegaly),Inappropriate GH Secretion Syndrome (Acromegaly),Hypersecretion Syndrome, Somatotropin (Acromegaly),Hypersecretion Syndromes, Somatotropin (Acromegaly),Somatotropin Hypersecretion Syndromes (Acromegaly),Syndrome, Somatotropin Hypersecretion (Acromegaly),Syndromes, Somatotropin Hypersecretion (Acromegaly)
D000224	Addison Disease	An adrenal disease characterized by the progressive destruction of the ADRENAL CORTEX, resulting in insufficient production of ALDOSTERONE and HYDROCORTISONE. Clinical symptoms include ANOREXIA; NAUSEA; WEIGHT LOSS; MUSCLE WEAKNESS; and HYPERPIGMENTATION of the SKIN due to increase in circulating levels of ACTH precursor hormone which stimulates MELANOCYTES.	Addison's Disease,Primary Adrenal Insufficiency,Primary Adrenocortical Insufficiency,Primary Hypoadrenalism,Addisons Disease,Adrenal Insufficiency, Primary,Adrenocortical Insufficiencies, Primary,Adrenocortical Insufficiency, Primary,Disease, Addison,Hypoadrenalism, Primary,Hypoadrenalisms, Primary,Insufficiencies, Primary Adrenocortical,Insufficiency, Primary Adrenocortical,Primary Adrenocortical Insufficiencies
D000309	Adrenal Insufficiency	Conditions in which the production of adrenal CORTICOSTEROIDS falls below the requirement of the body. Adrenal insufficiency can be caused by defects in the ADRENAL GLANDS, the PITUITARY GLAND, or the HYPOTHALAMUS.	Adrenal Gland Hypofunction,Hypoadrenalism,Adrenal Insufficiencies,Hypofunction, Adrenal Gland
D015068	17-Ketosteroids	Steroids that contain a ketone group at position 17.	17-Oxosteroids,17 Ketosteroids,17 Oxosteroids

Related Publications

A S GRINSHPUN

[Urinary 17-ketosteroids in various endocrine diseases].

January 1957, Problemy endokrinologii i gormonoterapii,

A S GRINSHPUN

[Excretion of 17-ketosteroids in normal conditions and in certain endocrine diseases].

January 1956, Postepy wiedzy medycznej,

A S GRINSHPUN

[17-Ketosteroids in various diseases].

January 1957, Izvestiia na meditsinskite instituti. [Bulletin des instituts de medecine]. Bulgarska akademiia na naukite. Otdelenie za biologicheski i meditsinski nauki,

A S GRINSHPUN

[STUDIES ON URINARY EXCRETION OF 17-KETOSTEROIDS IN INFANCY AND CHILDHOOD. 2. URINARY EXCRETION OF 17-KETOSTEROIDS IN VARIOUS PEDIATRIC DISEASES].

October 1963, Nihon Naibunpi Gakkai zasshi,

A S GRINSHPUN

Urinary 17-ketosteroids in various endocrine disorders.

February 1959, Clinical chemistry,

A S GRINSHPUN

Excretion of glycogenic corticoids and of 17-ketosteroids in various endocrine and other disorders.

February 1947, The Journal of clinical endocrinology and metabolism,

A S GRINSHPUN

Vaginal endocrine cytology and 17-ketosteroids urinary excretion.

January 1967, Maternidade e infancia; arquivos medicos-sociais,