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HexA Deficiency -- See Tay-Sachs Disease

An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry

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Hexachlorobenzene -- Environmental aspects. : Sixty Thousand Barrels / Director: Castle, Jane

2002

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Hexachlorobenzene -- Toxicology. : 7.30: 28/07/14

2014

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Hexachloroethane -- Toxicology

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Hexactinellida. : Zoology. Volume XXI

1887

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Hexadienoic acid -- See Sorbic acid

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Hexagons.

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Hexagons -- Teaching aids : Hexagrams [game] / Kenneth Saunders

1983

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Hexahydrobenzene -- See Cyclohexane

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Hexahydrothymol -- See Menthol

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Hexameter.

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Hexamethylene -- See Cyclohexane

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Hexamethylenebischlorophenylbiguanide -- See Chlorhexidine

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Hexamitidae -- See Also the narrower term Giardia

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Hexanaphthene -- See Cyclohexane

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Hexane -- See Also the narrower term Ketamine

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Hexane hexol -- See Mannitol

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Hexanehexol -- See Mannitol

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Hexapla. : Christianity and the transformation of the book : Origen, Eusebius, and the Library of Caesarea / Anthony Grafton, Megan Williams

2008

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Hexapoda -- See Insects

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Hexaprotodon -- See Also the narrower term Pygmy hippopotamus

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Hexaprotodon liberiensis -- See Pygmy hippopotamus

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Hexateuch -- See Bible. Hexateuch

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Hexe

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Hexe Motiv

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Hexenglaube

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Hexenprozess

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Hexenverfolgung

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Eichstätt (Bistum) -- Hexenverfolgung -- Sozialgeschichte -- 1590-1630. : Witchcraft, gender, and society in early modern Germany / by Jonathan B. Durrant

2007

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Hexenverfolgung -- Geschlechterrolle -- Deutschland -- Eichstätt (Bistum) -- Geschichte -- 1590-1630. : Witchcraft, gender, and society in early modern Germany / by Jonathan B. Durrant

2007

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Hexerei

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National parks and reserves -- Australia -- Victoria -- Hexham -- Management : Ridge Paddock addition to the Cobra Killuc Wildlife Reserve management statement

2005

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Hexiao, 1792-1871 -- See Herschel, John F. W. (John Frederick William), 1792-1871

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Hexogen -- See RDX (Cyclonite)

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Hexokinase -- See Glucokinase

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Hexokinase : Glucokinase and glycemic disease : from basics to novel therapeutics / volume editors, F.M. Matschinsky, M.A. Magnuson

2004

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Hexokinase D -- See Glucokinase

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Hexokinase type IV -- See Glucokinase

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Hexosamines -- See Also the narrower term Glucosamine

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Hexosaminidase -- See Hexosaminidases

Enzymes that catalyze the hydrolysis of N-acylhexosamine residues in N-acylhexosamides. Hexosaminidases also act on GLUCOSIDES; GALACTOSIDES; and several OLIGOSACCHARIDES

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Hexosaminidase A -- See Also Tay-Sachs Disease

An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry

1

Hexosaminidase A Deficiency -- See Tay-Sachs Disease

An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry

1

Hexosaminidase A Deficiency Disease -- See Tay-Sachs Disease

An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry

1

Hexosaminidase A deficiency (Tay-Sachs) -- See Tay-Sachs disease

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Hexosaminidase alpha-Subunit Deficiency (Variant B) -- See Tay-Sachs Disease

An autosomal recessive neurodegenerative disorder characterized by the onset in infancy of an exaggerated startle response, followed by paralysis, dementia, and blindness. It is caused by mutation in the alpha subunit of the HEXOSAMINIDASE A resulting in lipid-laden ganglion cells. It is also known as the B variant (with increased HEXOSAMINIDASE B but absence of hexosaminidase A) and is strongly associated with Ashkenazic Jewish ancestry

1

Hexose phosphates -- See Also the narrower term Inositol phosphates

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Hexoses : Nanomaterials in glucose sensing / Krishna Burugapalli, Ning Wang, Jakub Trzebinski, Wenhui Song, Anthony Cass

2014

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Hexter, Jack H., 1910-1996 -- See Hexter, J. H. (Jack H.), 1910-1996

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Hexter, Maurice Beck, 1891-1990. : Economic theory by Taussig, Young, and Carver at Harvard / edited by Marianne Johnson, Warren J. Samuels

2010

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