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Effects of HIV disease on lipid, glucose and insulin levels: results from a large antiretroviral‐naïve cohort

HIV medicine, 2005-03, Vol.6 (2), p.114-121

2005

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Protein Intake Is Positively Associated with Body Cell Mass in Weight-Stable HIV-Infected Men

The Journal of nutrition, 2003-04, Vol.133 (4), p.1143-1146

2003

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Effects of AAV-2-mediated aspartoacylase gene transfer in the tremor rat model of Canavan disease

Brain research. Molecular brain research., 2005-04, Vol.135 (1), p.112-121

2005

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Mucolipidosis IV: Morphology and Histochemistry of an Autopsy Case

Journal of neuropathology and experimental neurology, 1995-03, Vol.54 (2), p.154-164

1995

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Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: alpha-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy)

Bone marrow transplantation (Basingstoke), 2000-03, Vol.25 (5), p.541-544

2000

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Canine GM1-gangliosidosis. A clinical, morphologic, histochemical, and biochemical comparison of two different models

The American journal of pathology, 1992-03, Vol.140 (3), p.675-689

1992

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Dysmyelinogenesis in animal model of GM1 gangliosidosis

Pediatric neurology, 1992-07, Vol.8 (4), p.255-261

1992

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Adult-onset lysosomal storage disease in a Schipperke dog : clinical, morphological and biochemical studies

Acta neuropathologica, 1993-08, Vol.86 (3), p.306-312

1993

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Adult onset lysosomal storage disease in a Tibetan terrier : clinical, morphological and biochemical studies

Acta neuropathologica, 1992-11, Vol.84 (6), p.658-663

1992

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Leukocyte beta-glucosidase in homozygotes and heterozygotes for Gaucher disease

American journal of human genetics, 1980-03, Vol.32 (2), p.158-173

1980

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Neurovisceral and skeletal GM1-gangliosidosis in dogs with β-galactosidase deficiency

Science (American Association for the Advancement of Science), 1985-08, Vol.229 (4712), p.470-472

1985

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Animal models for lysosomal storage diseases: Their past and future contribution

Human pathology, 1989-09, Vol.20 (9), p.823-826

1989

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Morphology of leukocytes from cats affected with alpha-mannosidosis and mucopolysaccharidosis VI (MPS VI)

Veterinary pathology, 1989-07, Vol.26 (4), p.294

1989

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Leukocyte Sulfatidase for the Reliable Diagnosis of Metachromatic Leukodystrophy

Journal of neurochemistry, 1981-02, Vol.36 (2), p.724-731

1981

Volltextzugriff (PDF)

Oligosaccharides from placenta: early diagnosis of feline mannosidosis

FEBS letters, 1986-01, Vol.195 (1), p.247-252

1986

Volltextzugriff (PDF)

The Gaucher mouse

Biochemical and biophysical research communications, 1975-11, Vol.67 (1), p.85-90

1975

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Biochemical, ultrastructural and histochemical studies of cat placentae deficient in activity of lysosomal α-mannosidase

Placenta (Eastbourne), 1987-09, Vol.8 (5), p.545-553

1987

Volltextzugriff (PDF)

Deuteron Form Factors with Soft-Core Potentials

Progress of theoretical physics, 1973-06, Vol.49 (6), p.2135-2137, Article 2135

Raghavan, S. Srinivasa

1973

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Isolation and characterization of glucosylsphingosine from Gaucher's spleen

Journal of lipid research, 1974-09, Vol.15 (5), p.484-490

1974

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Studies on the positional integrity of glyceride fatty acids during digestion and absorption in rats

Biochemical journal, 1969-06, Vol.113 (1), p.81-87

1969

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HYDROLYTIC AND TRANSGLUCOLYTIC ACTIVITIES OF A PARTIALLY PURIFIED CALF BRAIN β‐GLUCOSIDASE

Journal of neurochemistry, 1976-10, Vol.27 (4), p.943-948

1976

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Deficiency of glucosylsphingosine: -Glucosidase in Gaucher disease

Biochemical and biophysical research communications, 1973-01, Vol.54 (1), p.256-263

1973

Volltextzugriff (PDF)

Abnormal copper metabolism in Menke's steely-hair syndrome

Pediatric research, 1979-07, Vol.13 (7), p.845-850

1979

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Deficiency of steroid β-glucosidase in Gaucher disease

Biochemical and biophysical research communications, 1975-11, Vol.67 (2), p.683-688

1975

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Purification of β-glucosidase activities from bovine spleen by affinity chromatography

Analytical biochemistry, 1974-07, Vol.60 (1), p.200-205

1974

Volltextzugriff (PDF)

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Effects of HIV disease on lipid, glucose and insulin levels: results from a large antiretroviral‐naïve cohort

Protein Intake Is Positively Associated with Body Cell Mass in Weight-Stable HIV-Infected Men

Effects of AAV-2-mediated aspartoacylase gene transfer in the tremor rat model of Canavan disease

Mucolipidosis IV: Morphology and Histochemistry of an Autopsy Case

Measurements from normal umbilical cord blood of four lysosomal enzymatic activities: alpha-L-iduronidase (Hurler), galactocerebrosidase (globoid cell leukodystrophy), arylsulfatase A (metachromatic leukodystrophy), arylsulfatase B (Maroteaux-Lamy)

Canine GM1-gangliosidosis. A clinical, morphologic, histochemical, and biochemical comparison of two different models

Dysmyelinogenesis in animal model of GM1 gangliosidosis

Adult-onset lysosomal storage disease in a Schipperke dog : clinical, morphological and biochemical studies

Adult onset lysosomal storage disease in a Tibetan terrier : clinical, morphological and biochemical studies

Leukocyte beta-glucosidase in homozygotes and heterozygotes for Gaucher disease

Neurovisceral and skeletal GM1-gangliosidosis in dogs with β-galactosidase deficiency

Animal models for lysosomal storage diseases: Their past and future contribution

Morphology of leukocytes from cats affected with alpha-mannosidosis and mucopolysaccharidosis VI (MPS VI)

Leukocyte Sulfatidase for the Reliable Diagnosis of Metachromatic Leukodystrophy

Oligosaccharides from placenta: early diagnosis of feline mannosidosis

The Gaucher mouse

Biochemical, ultrastructural and histochemical studies of cat placentae deficient in activity of lysosomal α-mannosidase

Deuteron Form Factors with Soft-Core Potentials

Isolation and characterization of glucosylsphingosine from Gaucher's spleen

Studies on the positional integrity of glyceride fatty acids during digestion and absorption in rats

HYDROLYTIC AND TRANSGLUCOLYTIC ACTIVITIES OF A PARTIALLY PURIFIED CALF BRAIN β‐GLUCOSIDASE

Deficiency of glucosylsphingosine: -Glucosidase in Gaucher disease

Abnormal copper metabolism in Menke's steely-hair syndrome

Deficiency of steroid β-glucosidase in Gaucher disease

Purification of β-glucosidase activities from bovine spleen by affinity chromatography

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