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  Hypogammaglobulinemia -- 2 Related Subjects   2
 

Hypogammaglobulinemias -- See Agammaglobulinemia


An immunologic deficiency state characterized by an extremely low level of generally all classes of gamma-globulin in the blood
  1
 

Hypogeous fungi -- See Also Soil fungi


  1
Hypoglossal nerve -- Testing : Nursing Assessment. The Nervous System. Objective Data. Hypoglossal Nerves / [produced by Medcom, Inc.]  2012 1
  Hypoglycemia -- 2 Related Subjects   2
Hypoglycemia.   17
Hypoglycemia -- chemically induced.   2
Hypoglycemia -- complications   2
Hypoglycemia -- Diet therapy.   2
Hypoglycemia -- Diet therapy -- Recipes.   2
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 in newborn infants. : Assessment of the newborn. Physical anomalies and neurologic issues. Neonatal hypoglycemia / [Medcom ; produced by Classroom Productions, Inc. ; directors: Jim Harrigan, Robert Suderman]  2010 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 : Never Events and Hospital-Acquired Conditions. Prevention Practices. Poor glycemic control / [produced by Medcom, Inc.]  2009 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
Hypoglycemia -- Treatment : Diabetes in clinical practice. Glycemic emergencies / [produced by Medcom, inc.]  2004 1
  Hypoglycemic agents -- 2 Related Subjects   2
Hypoglycemic agents.   8
Hypoglycemic agents -- Development   2
Hypoglycemic agents industry.   2
Hypoglycemic Agents -- pharmacokinetics : Drug therapy for Type 2 Diabetes : an Adis pocket reference / Andrew J. Krentz, Bedfordshire & Hertfordshire Postgraduate Medical School, United Kingdom  2012 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   2
 

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
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
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