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Mark		Year	Entries
	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
	Gatty, Alfred, Mrs., 1809-1873. : Mrs. Gatty and Mrs. Ewing / Christabel Maxwell	1949	1
	Gatty, Margaret, 1809-1873 -- See Gatty, Alfred, Mrs., 1809-1873		1
	Gatwick, Eng -- See Gatwick (England)		1
	Gatwick (England) : 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
	Gaucher disease.		5
	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 -- genetics. : Acid beta-Glucosidase/Glucocerebrosidase (GCase) / Gregory Grabowski	2016	1
	Gaucher Disease -- immunology. : Gaucher disease : from lysosomal storage to immunopathology / Hans Aerts	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 -- physiopathology. : Acid beta-Glucosidase/Glucocerebrosidase (GCase) / Gregory Grabowski	2016	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.		2
	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
	Gaucher Disease Type 3 -- 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 I -- 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 II -- 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 III -- 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-Schlagenhaufer syndrome -- See Gaucher disease		1
	Gaucher Splenomegaly -- 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 Syndrome -- 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's disease -- 2 Related Subjects		2
	Gauchers Diseases -- 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
	Gauchet, Marcel -- Interviews. : What is to be done? : a dialogue on communism, capitalism, and the future of democracy / Alain Badiou and Marcel Gauchet ; moderated by Martin Duru and Martin Legros ; translated by Susan Spitzer	2016	1
	Gauchos -- See Also Cowboys		1
	Gaucho's.		3
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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

Gaucher Disease Type 3 -- See Gaucher Disease

Gaucher Disease, Type I -- See Gaucher Disease

Gaucher Disease, Type II -- See Gaucher Disease

Gaucher Disease, Type III -- See Gaucher Disease

Gaucher-Schlagenhaufer syndrome -- See Gaucher disease

Gaucher Splenomegaly -- See Gaucher Disease

Gaucher Syndrome -- See Gaucher Disease

Gauchers Diseases -- See Gaucher Disease

Gauchos -- See Also Cowboys