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Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutations

Neurology, 1997-12, Vol.49 (6), p.1655-1661

1997

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Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California

Molecular genetics and metabolism, 2017-11, Vol.122 (3), p.76-84

2017

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Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy

Gene therapy, 2015-02, Vol.22 (2), p.111-115

2015

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AAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouse

Gene therapy, 2013-08, Vol.20 (8), p.785-796

2013

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Cloning and Characterization of the Human Type II Arginase Gene

Genomics (San Diego, Calif.), 1996-12, Vol.38 (2), p.118-123

1996

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Hyperargininemia due to liver arginase deficiency

Molecular genetics and metabolism, 2005-03, Vol.84 (3), p.243-251

2005

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Arginases I and II: do their functions overlap?

Molecular genetics and metabolism, 2004-04, Vol.81, p.38-44

2004

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Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy

Gene therapy, 2015-02, Vol.22 (2), p.216-216

2015

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Mouse Model for Human Arginase Deficiency

Molecular and Cellular Biology, 2002-07, Vol.22 (13), p.4491-4498

2002

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Helicobacter pylori Induces Macrophage Apoptosis by Activation of Arginase II

The Journal of immunology (1950), 2002-05, Vol.168 (9), p.4692-4700

2002

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SIDS and disorders of fatty acid oxidation: Where do we go from here?

The Journal of pediatrics, 1998-06, Vol.132 (6), p.913-914

Cederbaum, Stephen D.

1998

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Comparative properties of arginases

Comparative Biochemistry and Physiology Part B: Biochemistry and Molecular Biology, 1996-05, Vol.114 (1), p.107-132

1996

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Successful pregnancy outcome in a woman with argininosuccinate lyase deficiency

Journal of inherited metabolic disease, 1999-04, Vol.22 (2), p.102-106

1999

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Spontaneous pneumothorax in association with pyridoxine‐responsive homocystinuria

Journal of inherited metabolic disease, 1997-11, Vol.20 (6), p.831-832

1997

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VOIDING DYSFUNCTION IN A MOTHER AND DAUGHTER WITH MITOCHONDRIAL CYTOPATHY

The Journal of urology, 1998-09, Vol.160 (3), p.830-830

1998

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Expression of arginase isozymes in mouse brain

Journal of neuroscience research, 2001-11, Vol.66 (3), p.406-422

2001

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Laboratory evaluation of urea cycle disorders

The Journal of pediatrics, 2001-01, Vol.138 (1), p.S21-S29

2001

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Arginase induction by sodium phenylbutyrate in mouse tissues and human cell lines

Molecular genetics and metabolism, 2007, Vol.90 (1), p.37-41

2007

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Psychosocial issues and coping strategies in families affected by urea cycle disorders

The Journal of pediatrics, 2001-01, Vol.138 (1), p.S72-S80

2001

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Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapy

Pediatric research, 1990-03, Vol.27 (3), p.297-303

1990

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Differential expression of the two human arginase genes in hyperargininemia: enzymatic, pathologic, and molecular analysis

The Journal of clinical investigation, 1989-02, Vol.83 (2), p.602-609

1989

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Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme

Human genetics, 1993-03, Vol.91 (1), p.1-5

1993

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Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO production

American journal of physiology. Heart and circulatory physiology, 1996-11, Vol.271 (5), p.H1988-H1998

1996

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The gene for human liver arginase (ARG1) is assigned to chromosome band 6Q23

American journal of human genetics, 1986-08, Vol.39 (2), p.186-193

1986

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Molecular genetic study of human arginase deficiency

American journal of human genetics, 1992-06, Vol.50 (6), p.1281-1290

1992

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Outcome of pyruvate dehydrogenase deficiency treated with ketogenic diets. Studies in patients with identical mutations

Biochemical characteristics of newborns with carnitine transporter defect identified by newborn screening in California

Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy

AAV-based gene therapy prevents neuropathology and results in normal cognitive development in the hyperargininemic mouse

Cloning and Characterization of the Human Type II Arginase Gene

Hyperargininemia due to liver arginase deficiency

Arginases I and II: do their functions overlap?

Minimal ureagenesis is necessary for survival in the murine model of hyperargininemia treated by AAV-based gene therapy

Mouse Model for Human Arginase Deficiency

Helicobacter pylori Induces Macrophage Apoptosis by Activation of Arginase II

SIDS and disorders of fatty acid oxidation: Where do we go from here?

Comparative properties of arginases

Successful pregnancy outcome in a woman with argininosuccinate lyase deficiency

Spontaneous pneumothorax in association with pyridoxine‐responsive homocystinuria

VOIDING DYSFUNCTION IN A MOTHER AND DAUGHTER WITH MITOCHONDRIAL CYTOPATHY

Expression of arginase isozymes in mouse brain

Laboratory evaluation of urea cycle disorders

Arginase induction by sodium phenylbutyrate in mouse tissues and human cell lines

Psychosocial issues and coping strategies in families affected by urea cycle disorders

Guanidino compound analysis as a complementary diagnostic parameter for hyperargininemia: follow-up of guanidino compound levels during therapy

Differential expression of the two human arginase genes in hyperargininemia: enzymatic, pathologic, and molecular analysis

Arginase deficiency manifesting delayed clinical sequelae and induction of a kidney arginase isozyme

Arginase activity in endothelial cells: inhibition by NG-hydroxy-L-arginine during high-output NO production

The gene for human liver arginase (ARG1) is assigned to chromosome band 6Q23

Molecular genetic study of human arginase deficiency

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