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Mark		Year	Entries
	Gatto, Florence Terranova (1939-) : The scent of jasmine : vignettes from a Sicilian heritage / Florence Terranova Gatto	2007	1
	Gatto, John Taylor. : Dumbing us down : the hidden curriculum of compulsory schooling / John Taylor Gatto	1992	1
	Crime -- Australia -- Gatton : The Gatton mystery / James and Desmond Gibney	1977	1
	Criminals -- Australia -- Gatton : The Gatton mystery / James and Desmond Gibney	1977	1
	Murder -- Australia -- Gatton : The Gatton mystery / James and Desmond Gibney	1977	1
	Murder -- Australia -- Queensland -- Gatton		2
	Murder -- Investigation -- Australia -- Queensland -- Gatton -- Case studies : The Gatton murders : a true story of lust, vengeance and vile retribution / Stephanie Bennett	2004	1
	Murder -- Australia -- Gatton(Qld.) : The Gatton mystery / James and Desmond Gibney	1977	1
	Tomasi di Lampedusa, Giuseppe, 1896-1957. Gattopardo. English. : Novels for students. Volume 44 : presenting analysis, context, and criticism on commonly studied novels / Sara Constantakis, project editor ; foreword by Anne Devereaux Jordan	2014	1
	Visconti, Luchino, 1906-1976. Gattopardo : Il gattopardo : Luchino Visconti / Maddalena Angelino	2004	1
	Gattung		3
	Gattungstheorie		11
	Gatty, Alfred, Mrs., 1809-1873.		2
	Gatty, Margaret, 1809-1873 -- See Gatty, Alfred, Mrs., 1809-1873		1
	Gatuförsäljning. : City of noise : sound and nineteenth-century Paris / Aimée Boutin	2015	1
	Gatukonst -- Förenta staterna -- Kalifornien -- 1945- : Walls of empowerment : Chicana/o indigenist murals of California / Guisela Latorre	2008	1
	Gatuliv -- historia. : City of noise : sound and nineteenth-century Paris / Aimée Boutin	2015	1
	Gatuplanering. : Transit street design guide / National Association of City Transportation Officials	2016	1
	Gatwick, Eng -- See Gatwick (England)		1
	Gatwick (England) -- Newspapers. : Gatwick and Horley mirror (Gatwick, England)		1
	Gatwick (Surrey) -- See Gatwick (England)		1
	Gatzogiannē, Helenē -- See Gatzoyiannis, Eleni		1
	Gatzoyiannis, Eleni.		2
	Gauche divine (Group of artists) -- See Also Arts, Spanish 20th century		1
	Gauche (Politique)		2
	Gauche (politique) -- Etats-Unis. : Living inside our hope : a steadfast radical's thoughts on rebuilding the movement / Staughton Lynd	1997	1
	Gauche (science politique) -- États-Unis. : There's something happening here : the New Left, the Klan, and FBI counterintelligence / David Cunningham	2004	1
	Gauche (science politique) -- États-Unis -- 20e siècle. : Liberalism and its discontents / Alan Brinkley	1998	1
	Gauche (science politique) -- États-Unis -- 1969-1981. : Solidarity blues : race, culture, and the American left / Richard Iton	2000	1
	Gauche (science politique) -- Pays de l'Union européenne. : The Palgrave Handbook of Social Democracy in the European Union	2016	1
	Gaucher disease		2
	Gaucher Disease, Acute Neuronopathic -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Acute Neuronopathic Type -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Chronic -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Chronic Neuronopathic Type -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher disease -- Diagnosis : Advances in Gaucher disease : basic and clinical perspectives / editor, Gregory A. Grabowski	2013	1
	Gaucher Disease, Infantile -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Infantile Cerebral -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Juvenile -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Juvenile and Adult, Cerebral -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Neuronopathic -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Non-Neuronopathic -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Non Neuronopathic Form -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Noncerebral Juvenile -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Subacute Neuronopathic Form -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Subacute Neuronopathic Type -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease -- therapy : Advances in Gaucher disease : basic and clinical perspectives / editor, Gregory A. Grabowski	2013	1
	Gaucher disease -- Treatment : Advances in Gaucher disease : basic and clinical perspectives / editor, Gregory A. Grabowski	2013	1
	Gaucher Disease, Type 1 -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
	Gaucher Disease, Type 2 -- See Gaucher Disease An autosomal recessive disorder caused by a deficiency of acid beta-glucosidase (GLUCOSYLCERAMIDASE) leading to intralysosomal accumulation of glycosylceramide mainly in cells of the MONONUCLEAR PHAGOCYTE SYSTEM. The characteristic Gaucher cells, glycosphingolipid-filled HISTIOCYTES, displace normal cells in BONE MARROW and visceral organs causing skeletal deterioration, hepatosplenomegaly, and organ dysfunction. There are several subtypes based on the presence and severity of neurological involvement		1
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Gatty, Margaret, 1809-1873 -- See Gatty, Alfred, Mrs., 1809-1873

Gatwick, Eng -- See Gatwick (England)

Gatwick (Surrey) -- See Gatwick (England)

Gatzogiannē, Helenē -- See Gatzoyiannis, Eleni

Gauche divine (Group of artists) -- See Also Arts, Spanish 20th century

Gaucher Disease, Acute Neuronopathic -- See Gaucher Disease

Gaucher Disease, Acute Neuronopathic Type -- See Gaucher Disease

Gaucher Disease, Chronic -- See Gaucher Disease

Gaucher Disease, Chronic Neuronopathic Type -- See Gaucher Disease

Gaucher Disease, Infantile -- See Gaucher Disease

Gaucher Disease, Infantile Cerebral -- See Gaucher Disease

Gaucher Disease, Juvenile -- See Gaucher Disease

Gaucher Disease, Juvenile and Adult, Cerebral -- See Gaucher Disease

Gaucher Disease, Neuronopathic -- See Gaucher Disease

Gaucher Disease, Non-Neuronopathic -- See Gaucher Disease

Gaucher Disease, Non Neuronopathic Form -- See Gaucher Disease

Gaucher Disease, Noncerebral Juvenile -- See Gaucher Disease

Gaucher Disease, Subacute Neuronopathic Form -- See Gaucher Disease

Gaucher Disease, Subacute Neuronopathic Type -- See Gaucher Disease

Gaucher Disease, Type 1 -- See Gaucher Disease

Gaucher Disease, Type 2 -- See Gaucher Disease