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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
Hypoglykämie : Monogenic hyperinsulinemic hypoglycemia disorders / volume editors, Charles A. Stanley, Diva D. De León  2012 1
Hypoglykämie -- Humaninsulin. : Insulin : a voice for choice / Arthur Teuscher  2007 1
Hypoglykemi. : Monogenic hyperinsulinemic hypoglycemia disorders / volume editors, Charles A. Stanley, Diva D. De León  2012 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
Hypokinesia -- Treatment : Sport und Bewegungserziehung in der Suchtarbeit : Sozialpädagogische und dialogisch-philosophische Aspekte in der Suchtprävention und Behandlung von Kindern und Jugendlichen  2012 1
 

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
 

Hypolipidemic agents -- See Antilipemic agents


  1
Hypolipidemic Agents : Atherosclerosis : diet and drugs / editor, Arnold von Eckardstein ; contributors, J. Ahrens [and others]  2005 1
Hypolipidemic Agents -- therapeutic use.   2
 

Hypolipidemic Drugs -- See Hypolipidemic Agents


Substances that lower the levels of certain LIPIDS in the BLOOD. They are used to treat HYPERLIPIDEMIAS
  1
 

Hypolipoproteinemias -- See Also Lipoproteins


Lipid-protein complexes involved in the transportation and metabolism of lipids in the body. They are spherical particles consisting of a hydrophobic core of TRIGLYCERIDES and CHOLESTEROL ESTERS surrounded by a layer of hydrophilic free CHOLESTEROL; PHOSPHOLIPIDS; and APOLIPOPROTEINS. Lipoproteins are classified by their varying buoyant density and sizes
  1
Hypomania   15
Hypomania -- Case studies   14
Hypomania -- Handbooks, manuals, etc. : The hypomania handbook : the challenge of elevated mood / Christopher M. Doran  2007 1
 

Hypomenorrhea -- See Menstruation Disturbances


Variations of MENSTRUATION which may be indicative of disease
  1
 

Hypomyotonia -- See Muscle Hypotonia


A diminution of the skeletal muscle tone marked by a diminished resistance to passive stretching
  1
Hyponatremia   2
Hyponatremia -- Diagnosis : Hyponatremia : evaluation and treatment / Eric E. Simon, editor  2013 1
Hyponatremia -- Prevention : Heat illness in athletes : prevention, recognition, and treatment / presented by W. Larry Kenney  2013 1
Hyponatremia -- therapy   2
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