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Hypoglycemia -- Early detection : Human-canine collaboration in care : doing diabetes / Fenella Eason  2020 1
Hypoglycemia -- etiology.   2
 

Hypoglycemia, Fasting -- See Hypoglycemia


A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH
  1
Hypoglycemia -- Pathophysiology. : Hypoglycaemia in clinical diabetes / edited by Brian M. Frier and B. Miles Fisher  1999 1
Hypoglycemia -- physiopathology.   3
 

Hypoglycemia, Postabsorptive -- See Hypoglycemia


A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH
  1
 

Hypoglycemia, Postprandial -- See Hypoglycemia


A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH
  1
Hypoglycemia -- prevention & control. : Type 1 diabetes : clinical management of the athlete / Ian Gallen, editor  2012 1
 

Hypoglycemia, Reactive -- See Hypoglycemia


A syndrome of abnormally low BLOOD GLUCOSE level. Clinical hypoglycemia has diverse etiologies. Severe hypoglycemia eventually lead to glucose deprivation of the CENTRAL NERVOUS SYSTEM resulting in HUNGER; SWEATING; PARESTHESIA; impaired mental function; SEIZURES; COMA; and even DEATH
  1
  Hypoglycemic agents -- 2 Related Subjects   2
Hypoglycemic agents.   4
Hypoglycemic agents -- Development   2
Hypoglycemic agents industry. : Insulin : a voice for choice / Arthur Teuscher  2007 1
Hypoglycemic agents -- Pharmacokinetics -- Congresses. : Pharmacokinetics and mode of action of oral hypoglycemic agents. Farmacocinetica e meccanismo d'azione degli ipoglicemizzanti orali. III Capri Conference, 2-3 IV 1969  1969 1
Hypoglycemic agents -- Side effects.   2
Hypoglycemic Agents -- therapeutic use. : Pharmacotherapy of diabetes : new developments : improving life and prognosis for diabetic patients / edited by Carl Erik Mogensen  2007 1
 

Hypoglycemic Drugs -- See Hypoglycemic Agents


Substances which lower blood glucose levels
  1
 

Hypoglycemic Effect -- See Hypoglycemic Agents


Substances which lower blood glucose levels
  1
 

Hypoglycemic Effects -- See Hypoglycemic Agents


Substances which lower blood glucose levels
  1
 

Hypoglycemics -- See Hypoglycemic Agents


Substances which lower blood glucose levels
  1
 

Hypoglycemosis -- See Hypoglycemia


  1
 

Hypoglycin A -- See Also the narrower term Hypoglycemia


  1
Hypogonadism.   6
 

Hypogonadism, Anosmic -- See Kallmann Syndrome


A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
  1
Hypogonadism -- genetics. : Kallmann syndrome and hypogonadotropic hypogonadism / volume editor, Richard Quinton  2010 1
 

Hypogonadism, Hypergonadotropic -- See Hypogonadism


Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism)
  1
 

Hypogonadism, Hypogonadotropic -- See Hypogonadism


Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism)
  1
 

Hypogonadism, Isolated Hypogonadotropic -- See Hypogonadism


Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism)
  1
Hypogonadism -- physiopathology. : Testosterone deficiency in men / edited by T. Hugh Jones  2008 1
 

Hypogonadisms, Anosmic -- See Kallmann Syndrome


A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
  1
 

Hypogonadotropic Hypogonadism -- See Hypogonadism


Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism)
  1
 

Hypogonadotropic Hypogonadism and Anosmia -- See Kallmann Syndrome


A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
  1
 

Hypogonadotropic Hypogonadism, Anosmia, and Midline Cranial Anomalies (Cleft Lip, Cleft Palate and Imperfect Fusion) -- See Kallmann Syndrome


A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
  1
 

Hypogonadotropic Hypogonadism-Anosmia Syndrome -- See Kallmann Syndrome


A genetically heterogeneous disorder caused by hypothalamic GNRH deficiency and OLFACTORY NERVE defects. It is characterized by congenital HYPOGONADOTROPIC HYPOGONADISM and ANOSMIA, possibly with additional midline defects. It can be transmitted as an X-linked (GENETIC DISEASES, X-LINKED), an autosomal dominant, or an autosomal recessive trait
  1
 

Hypogrammidae -- See Noctuidae


  1
Hypographs : Introduction to graph and hypergraph theory / Vitaly I. Voloshin  2009 1
 

Hypogravity -- See Also Weightlessness


Condition in which no acceleration, whether due to gravity or any other force, can be detected by an observer within a system. It also means the absence of weight or the absence of the force of gravity acting on a body. Microgravity, gravitational force between 0 and 10 -6 g, is included here. (From NASA Thesaurus, 1988)
  1
Hypogravity : NPJ microgravity  2015 1
 

Hypokalaemia -- See Hypokalemia


  1
Hypokalemia. : Hyperkalemia : new insights for the healtcare professional : scholarlypaper / Q. Ashton Acton, PhD, general editor  2012 1
 

Hypokaliaemia -- See Hypokalemia


  1
 

Hypokaliemia -- See Hypokalemia


  1
Hypokinesia.   4
 

Hypokinesia, Antiorthostatic -- See Hypokinesia


Slow or diminished movement of body musculature. It may be associated with BASAL GANGLIA DISEASES; MENTAL DISORDERS; prolonged inactivity due to illness; and other conditions
  1
Hypokinesia -- Australia.   2
 

Hypokinesias, Antiorthostatic -- See Hypokinesia


Slow or diminished movement of body musculature. It may be associated with BASAL GANGLIA DISEASES; MENTAL DISORDERS; prolonged inactivity due to illness; and other conditions
  1
  Hypolactasia -- 2 Related Subjects   2
Hypolimnetic aeration. : Manitoba Prairie Lakes : In-lake Remediation Treatment Summary / Kimberly Lewtas  2016 1
 

Hypolipemia -- See Also the narrower term Hypocholesteremia


  1
 

Hypolipemic agents -- See Antilipemic agents


  1
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