S. Raghavan

发表

Molecular basis of late‐life globoid cell leukodystrophy

R. De Gasperi, M. A. Gama Sosa, S. Battistini, 1999, Human mutation.

Bone marrow-derived mesenchymal stem cells remain host-derived despite successful hematopoietic engraftment after allogeneic transplantation in patients with lysosomal and peroxisomal storage diseases.

P. Watkins, S. Gerson, A. Caplan, 1999, Experimental hematology.

Globoid cell leukodystrophy (Krabbe disease): Normal umbilical cord blood galactocerebrosidase activity and polymorphic mutations

W. Krivit, G. Pastores, S. Raghavan, 2005, Journal of Inherited Metabolic Disease.

Dysmyelinogenesis in animal model of GM1 gangliosidosis.

J. Alroy, V. Runge, L. Adelman, 1992, Pediatric neurology.

Mucolipidosis IV: Morphology and Histochemistry of an Autopsy Case

R. Folkerth, J. Alroy, S. Raghavan, 1995, Journal of neuropathology and experimental neurology.

Rapid detection of three large novel deletions of the aspartoacylase gene in non-Jewish patients with Canavan disease.

P. Leone, G. Pastores, S. Raghavan, 2006, Molecular genetics and metabolism.

Mutation analysis of the aspartoacylase gene in non-Jewish patients with Canavan disease.

P. Leone, G. Pastores, S. Raghavan, 2006, Advances in experimental medicine and biology.

Isolation and characterization of the normal canine β-galactosidase gene and its mutation in a dog model of GM1-gangliosidosis

G. Johnson, J. Alroy, G. Pastores, 2000, Journal of Inherited Metabolic Disease.

Leukocyte beta-glucosidase in homozygotes and heterozygotes for Gaucher disease.

S. Raghavan, E. Kolodny, J. Topol, 1980, American journal of human genetics.

Deficiency of steroid β-glucosidase in Gaucher disease

R. Labow, J. Kanfer, S. Raghavan, 1975 .

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

J. Alroy, M. Natowicz, S. Schelling, 2004, Acta Neuropathologica.

Late-onset Krabbe disease (globoid cell leukodystrophy): clinical and biochemical features of 15 cases.

W. Krivit, S. Raghavan, E. Kolodny, 1991, Developmental neuroscience.

Isolation and characterization of glucosylsphingosine from Gaucher's spleen.

J. Kanfer, S. Raghavan, R. Mumford, 1974, Journal of lipid research.

Purification of beta-glucosidase activities from bovine spleen by affinity chromatography.

J. Byrd, J. Kanfer, S. Raghavan, 1974, Analytical biochemistry.

Deficiency of glucosylsphingosine: -Glucosidase in Gaucher disease

J. Kanfer, S. Raghavan, R. Mumford, 1973 .

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

J. Kanfer, S. Raghavan, R. Mumford, 1976, Journal of neurochemistry.

Hydrolytic and transglucosylation activities of a purified calf spleen beta-glucosidase.

J. Kanfer, S. Raghavan, R. Mumford, 1975, Biochimica et biophysica acta.

Synthesis of glucosylceramide by purified calf spleen β-glucosidase

J. Kanfer, S. Raghavan, R. Mumford, 1974 .

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

J. Alroy, C. Warren, S. Raghavan, 1989 .

Characterization of 6-hexadecanoylamino-4-methylumbelliferyl-beta-D- galactopyranoside as fluorogenic substrate of galactocerebrosidase for the diagnosis of Krabbe disease.

S. Raghavan, E. Kolodny, G. Wiederschain, 1992, Clinica chimica acta; international journal of clinical chemistry.

The effects of trypsin on purified myelin.

J. Kanfer, S. Raghavan, D. Rhoads, 1973, Biochimica et biophysica acta.

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

J. Wagner, W. Krivit, C. Peters, 2000, Bone Marrow Transplantation.

Late-onset G sub M2 gangliosidosis

R. De Gasperi, R. Gasperi, S. Battistini, 1996, Neurology.

Two abnormalities of hexosaminidase A in clinically normal individuals.

L. Jackson, S. Raghavan, E. Kolodny, 1986, American journal of human genetics.

GM2-gangliosidosis Hexosaminidase mutations not of the Tay-Sachs type procedure unusual clinical variants

S. Raghavan, E. Kolodny, 1983, Trends in Neurosciences.

Nonuniform Deficiency of Hexosaminidase A in Tissues and Fluids of Two Unrelated Individuals

H. Kazazian, G. Thomas, J. O'brien, 1982, Pediatric Research.

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

J. Alroy, S. Raghavan, R. Jakowski, 2004, Acta Neuropathologica.

GM1-ganglioside β-galactosidase in leukocytes and cultured fibroblasts

S. Raghavan, E. Kolodny, A. Gajewski, 1977 .

Clinical, neurophysiological, biochemical and morphological features of eyes in Persian cats with mannosidosis

J. Alroy, D. Albert, C. Warren, 1991, Virchows Archiv. B, Cell pathology including molecular pathology.

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

J. Alroy, C. Warren, S. Raghavan, 1992, The American journal of pathology.

Characterization of α-mannosidase in feline mannosidosis

J. Alroy, S. Raghavan, E. Kolodny, 1988, Journal of Inherited Metabolic Disease.

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

J. Alroy, C. Warren, S. Raghavan, 1987, Placenta.

Oligosaccharides from placenta: early diagnosis of feline mannosidosis

J. Alroy, C. Warren, S. Raghavan, 1986, FEBS letters.

Inherited lysosomal storage disease associated with deficiencies of β‐galactosidase and α‐neuraminidase in sheep

J. Opitz, S. Walkley, R. McCluer, 1988 .

Leukocyte Sulfatidase for the Reliable Diagnosis of Metachromatic Leukodystrophy

S. Raghavan, E. Kolodny, A. Gajewski, 1981, Journal of neurochemistry.

The Gaucher mouse.

J. Kanfer, S. Raghavan, R. Mumford, 1975, Biochemical and biophysical research communications.

GM2-ganglioside metabolism in hexosaminidase A deficiency states: determination in situ using labeled GM2 added to fibroblast cultures.

S. Raghavan, E. Kolodny, T. Lyerla, 1985, American journal of human genetics.

Intrathecal synthesis of anti-sulfatide IgG is associated with peripheral nerve disease in acquired immunodeficiency syndrome.

R. De Gasperi, S. Battistini, R. Patarca, 1996, AIDS research and human retroviruses.

Phenotypic manifestations of Gaucher disease: clinical features in 48 biochemically verified type 1 patients and comment on type 2 patients.

S. Raghavan, E. Kolodny, M. Ullman, 1982, Progress in clinical and biological research.

Results of a phase i clinical trial of allogeneic mesenchymal stem cell (msc) transplantation in patients with hurlerdisease and metachromaticleukodystrophy (mld)

S. Gerson, A. Caplan, H. Lazarus, 2000 .

Acid hydrolases in neuronal and glial enriched fractions of rat brain.

J. Kanfer, S. Raghavan, D. Rhoads, 1972, Biochimica et biophysica acta.

Ceramide galactoside of enriched neuronal and glial fractions from rat brain.

J. Kanfer, S. Raghavan, 1972, The Journal of biological chemistry.

Morphology of Leukocytes from Cats Affected with α-Mannosidosis and Mucopolysaccharidosis VI (MPS VI)

J. Alroy, S. Raghavan, V. Goyal, 1989, Veterinary pathology.

Purification and immunological characterization of acid beta-galactosidase from dog liver.

J. Alroy, S. Raghavan, S. Hotamisligil, 1993, Comparative biochemistry and physiology. B, Comparative biochemistry.

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

S. Raghavan, J. Ganguly, 1969, The Biochemical journal.

Neurovisceral and skeletal GM1-gangliosidosis in dogs with beta-galactosidase deficiency.

J. Alroy, C. Warren, S. Schelling, 1985, Science.

Mild‐onset presentation of Canavan's disease associated with novel G212A point mutation in aspartoacylase gene

D. Shera, Andrew Freese, L. Bilaniuk, 2006, Annals of neurology.

Identification and characterization of novel mutations of the aspartoacylase gene in non-Jewish patients with Canavan disease

R. De Gasperi, R. Gasperi, P. Leone, 2002, Journal of Inherited Metabolic Disease.

Spontaneous appearance of Tay-Sachs disease in an animal model.

J. Alroy, G. Pastores, S. Raghavan, 2008, Molecular genetics and metabolism.

Inherited lysosomal storage disease associated with deficiencies of beta-galactosidase and alpha-neuraminidase in sheep.

S. Walkley, R. McCluer, S. Raghavan, 1988, American journal of medical genetics.

LECTIN HISTOCHEMISTRY OF GLYCOLIPID STORAGE DISEASES ON FROZEN AND PARAFFIN SECTIONS

J. Alroy, A. Ucci, S. Raghavan, 1985 .

In vitro incorporation of ( 14 C)serine, ( 14 C)ethanolamine, and ( 14 C)choline into phospholipids of neuronal and glial-enriched fractions from rat brain by base exchange.

J. Kanfer, S. Raghavan, D. Rhoads, 1972, Journal of Biological Chemistry.