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Astrocyte Glutamine Synthetase: Importance in Hyperammonemic Syndromes and Potential Target for Therapy

Neurotherapeutics, 2010-10, Vol.7 (4), p.452-470

2010

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Survival after Treatment with Phenylacetate and Benzoate for Urea-Cycle Disorders

The New England journal of medicine, 2007-05, Vol.356 (22), p.2282-2292

2007

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Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis

The Journal of pediatrics, 1999-03, Vol.134 (3), p.268-272

1999

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Encephalopathy in acute liver failure resulting from acetaminophen intoxication: New observations with potential therapy

Critical care medicine, 2011-11, Vol.39 (11), p.2550-2553

2011

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Long-Term Treatment of Girls with Ornithine Transcarbamylase Deficiency

The New England journal of medicine, 1996-09, Vol.335 (12), p.855-860

1996

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Natural history of symptomatic partial ornithine transcarbamylase deficiency

The New England journal of medicine, 1986-02, Vol.314 (9), p.541

1986

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Preserved hypocapnic pial arteriolar constriction during hyperammonemia by glutamine synthetase inhibition

American journal of physiology. Heart and circulatory physiology, 1999-02, Vol.276 (2), p.H456-H463

1999

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Urea cycle disorders : Diagnosis, pathophysiology, and therapy

Advances in pediatrics, 1996, Vol.43 (1), p.127-170

1996

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Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies

The New England journal of medicine, 1984-06, Vol.310 (23), p.1500

1984

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Glutamine-dependent inhibition of pial arteriolar dilation to acetylcholine with and without hyperammonemia in the rat

American journal of physiology. Regulatory, integrative and comparative physiology, 2005-06, Vol.288 (6), p.R1612-R1619

2005

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Phenylacetylglutamine may replace urea as a vehicle for waste nitrogen excretion

Pediatric research, 1991-02, Vol.29 (2), p.147-150

BRUSILOW, S. W

1991

Volltextzugriff (PDF)

The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency

Medicine (Baltimore), 1998-11, Vol.77 (6), p.389-397

1998

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Induction of fetal hemoglobin synthesis in children with sickle cell anemia on low-dose oral sodium phenylbutyrate therapy

Journal of pediatric hematology/oncology, 2002-12, Vol.24 (9), p.737-741

2002

Volltextzugriff (PDF)

Methionine sulfoximine, a glutamine synthetase inhibitor, attenuates increased extracellular potassium activity during acute hyperammonemia

Journal of cerebral blood flow and metabolism, 1997-01, Vol.17 (1), p.44

1997

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Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus: A Cause of Postpartum Coma

The New England journal of medicine, 1990-06, Vol.322 (23), p.1652-1655

1990

Volltextzugriff (PDF)

Prospective treatment of urea cycle disorders

The Journal of pediatrics, 1991-12, Vol.119 (6), p.923-928

1991

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Waste nitrogen excretion via amino acid acylation: benzoate and phenylacetate in lysinuric protein intolerance

Pediatric research, 1986-11, Vol.20 (11), p.1117-1121

1986

Volltextzugriff (PDF)

Hypocapnia

The New England journal of medicine, 2002-11, Vol.347 (19), p.1533-1533

Carey, Brian J

2002

Volltextzugriff (PDF)

Interaction of glutamine and arginine on cerebrovascular reactivity to hypercapnia

American journal of physiology. Heart and circulatory physiology, 2000-05, Vol.278 (5), p.H1577-H1584

2000

Volltextzugriff (PDF)

Allopurinol-Induced Orotidinuria: A Test for Mutations at the Ornithine Carbamoyltransferase Locus in Women

The New England journal of medicine, 1990-06, Vol.322 (23), p.1641-1645

1990

Volltextzugriff (PDF)

Impaired pial arteriolar reactivity to hypercapnia during hyperammonemia depends on glutamine synthesis

Stroke (1970), 1996-04, Vol.27 (4), p.729-736

1996

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Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis

The New England journal of medicine, 1984-06, Vol.310 (25), p.1630

1984

Volltextzugriff (PDF)

Inborn errors of metabolism in children referred with Reye's syndrome. A changing pattern

JAMA : the journal of the American Medical Association, 1988-12, Vol.260 (21), p.3167

1988

Volltextzugriff (PDF)

Oral Sodium Phenylbutyrate Therapy in Homozygous β Thalassemia: A Clinical Trial

Blood, 1995-01, Vol.85 (1), p.43-49

1995

Volltextzugriff (PDF)

Hypocapnia

The New England journal of medicine, 2002-11, Vol.347 (19), p.1533; author reply 1533

Brusilow, Saul W

2002

Volltextzugriff (PDF)

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Astrocyte Glutamine Synthetase: Importance in Hyperammonemic Syndromes and Potential Target for Therapy

Survival after Treatment with Phenylacetate and Benzoate for Urea-Cycle Disorders

Neonatal onset ornithine transcarbamylase deficiency: A retrospective analysis

Encephalopathy in acute liver failure resulting from acetaminophen intoxication: New observations with potential therapy

Long-Term Treatment of Girls with Ornithine Transcarbamylase Deficiency

Natural history of symptomatic partial ornithine transcarbamylase deficiency

Preserved hypocapnic pial arteriolar constriction during hyperammonemia by glutamine synthetase inhibition

Urea cycle disorders : Diagnosis, pathophysiology, and therapy

Neurologic outcome in children with inborn errors of urea synthesis. Outcome of urea-cycle enzymopathies

Glutamine-dependent inhibition of pial arteriolar dilation to acetylcholine with and without hyperammonemia in the rat

Phenylacetylglutamine may replace urea as a vehicle for waste nitrogen excretion

The phenotype of ostensibly healthy women who are carriers for ornithine transcarbamylase deficiency

Induction of fetal hemoglobin synthesis in children with sickle cell anemia on low-dose oral sodium phenylbutyrate therapy

Methionine sulfoximine, a glutamine synthetase inhibitor, attenuates increased extracellular potassium activity during acute hyperammonemia

Hyperammonemia in Women with a Mutation at the Ornithine Carbamoyltransferase Locus: A Cause of Postpartum Coma

Prospective treatment of urea cycle disorders

Waste nitrogen excretion via amino acid acylation: benzoate and phenylacetate in lysinuric protein intolerance

Hypocapnia

Interaction of glutamine and arginine on cerebrovascular reactivity to hypercapnia

Allopurinol-Induced Orotidinuria: A Test for Mutations at the Ornithine Carbamoyltransferase Locus in Women

Impaired pial arteriolar reactivity to hypercapnia during hyperammonemia depends on glutamine synthesis

Treatment of episodic hyperammonemia in children with inborn errors of urea synthesis

Inborn errors of metabolism in children referred with Reye's syndrome. A changing pattern

Oral Sodium Phenylbutyrate Therapy in Homozygous β Thalassemia: A Clinical Trial

Hypocapnia

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