Mark L Batshaw


Ontology type: schema:Person     


Person Info

NAME

Mark L

SURNAME

Batshaw

Publications in SciGraph latest 50 shown

  • 2018-07-04 Transatlantic combined and comparative data analysis of 1095 patients with urea cycle disorders—a successful strategy for clinical research of rare diseases in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2016-07 Improving long term outcomes in urea cycle disorders-report from the Urea Cycle Disorders Consortium in JOURNAL OF INHERITED METABOLIC DISEASE
  • 2016-03 A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice in NATURE BIOTECHNOLOGY
  • 2012-04 Sustained correction of OTC deficiency in spf ash mice using optimized self-complementary AAV2/8 vectors in GENE THERAPY
  • 2009-07 Intellectual, Adaptive, and Behavioral Functioning in Children With Urea Cycle Disorders in PEDIATRIC RESEARCH
  • 2007-10 Poster Abstract #15: Preliminary Experience With MRS at 3T in Urea Cycle Disorders Detects Altered Metabolism in Partial Ornithine Transcarbamylase Deficiency in NEUROTHERAPEUTICS
  • 2002-07 Humoral Immune Response to Recombinant Adenovirus and Adeno-Associated Virus after In Utero Administration of Viral Vectors in Mice in PEDIATRIC RESEARCH
  • 2002-05 Recruitment and Development of Academic Pediatricians: Departmental Commitments to Promote Success in PEDIATRIC RESEARCH
  • 2000-12 Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors in GENE THERAPY
  • 2000-10 Correction of argininosuccinate synthetase (AS) deficiency in a murine model of citrullinemia with recombinant adenovirus carrying human AS cDNA in GENE THERAPY
  • 2000-10 Transient depletion of CD4 lymphocyte improves efficacy of repeated administration of recombinant adenovirus in the ornithine transcarbamylase deficient sparse fur mouse in GENE THERAPY
  • 1999-11 Correction of Ureagenesis after Gene Transfer in an Animal Model and after Liver Transplantation in Humans with Ornithine Transcarbamylase Deficiency in PEDIATRIC RESEARCH
  • 1999-04 Adeno-Associated Virus(AAV)-Mediated Expression of Ornithine Transcarbamylase (OTC) in OTC Deficient spf-ash mMice in PEDIATRIC RESEARCH
  • 1998-06 In vivo measurement of ureagenesis with stable isotopes in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1998-06 Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiency in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1998-04 Comparative toxicity of E4 deleted vectors expressing human ornithine transcarbamylase (OTC) cDNA ♦ 730 in PEDIATRIC RESEARCH
  • 1998-04 Phase I trial of adenoviral gene transfer in ornithine transcarbamylase deficiency † 731 in PEDIATRIC RESEARCH
  • 1998-04 Measuring Ureagenesis In Vivo with Stable Isotopes Provides a Tool to Assess Efficacy of Gene Therapy for Ornithine Transcarbamylase Deficiency ♦ 727 in PEDIATRIC RESEARCH
  • 1998-04 Detecting Heterozygotes for Ornithine Transcarbamylase Deficiency: Comparison of Allopurinol Loading Test With 15NH4 Loading Study† 744 in PEDIATRIC RESEARCH
  • 1997-04 Anti-CD4 Antibody Permits Readministration of Recombinant Adenovirus to Correct Ornithine Transcarbamylase Deficiency (OTCD) in the Sparse Fur(spf/Y) Mice. • 638 in PEDIATRIC RESEARCH
  • 1997-04 Adenovirus-Mediated in Vivo Gene Transfer Rapidly Protects Ornithine Transcarbamylase-Deficient Mice from an Ammonium Challenge in PEDIATRIC RESEARCH
  • 1997-04 In Vivo Gene Therapy Corrects Neurochemical Abnormalities in the Ornithine Transcarbamylase (OTC) Deficient Sparse Fur (spf/Y) Mouse. ♦ 1748 in PEDIATRIC RESEARCH
  • 1996-04 GENE THERAPY IN THE ORNITHINE TRANSCARBAMYLASE DEFICIENT MOUSE PREVENTS CLINICAL SEQUELAE OF NITROGEN CHALLENGE. ▴ 886 in PEDIATRIC RESEARCH
  • 1996-04 UREAGENESIS IN OTC HETEROZYGOTES: IN VIVO STUDIES WITH15 NH4Cl • 887 in PEDIATRIC RESEARCH
  • 1992-10 Quinolinate in Brain and Cerebrospinal Fluid in Rat Models of Congenital Hyperammonemia in PEDIATRIC RESEARCH
  • 1991 Inborn Errors of Amino Acid and Organic Acid Metabolism in PRINCIPLES OF PERINATAL-NEONATAL METABOLISM
  • 1988-04 Effect of Sodium Benzoate and Sodium Phenylacetate on Brain Serotonin Turnover in the Ornithine Transcarbamylase-Deficient Sparse-Fur Mouse in PEDIATRIC RESEARCH
  • 1987-04 SODIUM BENZOATE (SB) INCREASES FREE TRYPTOPHAN (TRP) IN BLOOD AND SEROTONIN (5-HT) FLUX IN CORTEX OF OTC DEFICIENT SPF MICE in PEDIATRIC RESEARCH
  • 1986-12 Behavioral and Neurotransmitter Changes in the Urease-Infused Rat: A Model of Congenital Hyperammonemia in PEDIATRIC RESEARCH
  • 1985-07 Long-Chain Acyl Coenzyme A Dehydrogenase Deficiency: An Inherited Cause of Nonketotic Hypoglycemia in PEDIATRIC RESEARCH
  • 1985-04 1252 NATURAL HISTORY AND DIAGNOSTIC DELAY IN PARTIAL ORNITHINE TRANSCARBAMYLASE DEFICIENCY (POTCD) in PEDIATRIC RESEARCH
  • 1984-06 Treatment of thecbl B form of methylmalonic acidaemia with adenosylcobalamin in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1984-04 MITOCHONDRIAL NADH - UBIQUINONE OXIDOREDUCTASE (Complex 1) DEFICIENCY IN AN INFANT WITH CONGENITAL LACTIC ACIDOSIS in PEDIATRIC RESEARCH
  • 1984-04 SEROTONIN AND ANOREXIA IN A PATIENT WITH ARGININOSUCCINASE (AL) DEFICIENCY in PEDIATRIC RESEARCH
  • 1982 Effects of Arginine-Free Meals on Ureagenesis in Cats in UREA CYCLE DISEASES
  • 1982 Therapy of Neonatal Onset Urea Cycle Enzymopathies (UCE) in UREA CYCLE DISEASES
  • 1981-12 Evidence of lack of toxicity of sodium phenylacetate and sodium benzoate in treating urea cycle enzymopathies in JOURNAL OF INHERITED METABOLIC DISEASE
  • 1981-04 87 LINGUISTIC DEVELOPMENT BETWEEN 12 AND 24 MONTHS: A COGNITIVE PREDICTOR in PEDIATRIC RESEARCH
  • 1981-04 1610 THE ASYMMETRICAL TONIC NECK REFLEX (ATNR): INFANT INDICATOR OF LATER DEVELOPMENT in PEDIATRIC RESEARCH
  • 1981-04 1159 DIAGNOSIS, TREATMENT AND FOLLOW UP OF NEONATAL ARGINOSUCCINIC ACIDEMIA in PEDIATRIC RESEARCH
  • 1981-04 61 BEHAVIORAL MEDICINE ASSESSMENT IN DySTONIA MUBOULORUM DEFORMANS in PEDIATRIC RESEARCH
  • 1981-04 1559 DEPAKENE (VPA) INDUCED HYPERAMMONEMIA (HA) in PEDIATRIC RESEARCH
  • 1980-12 Plasma α-Ketoglutarate in Urea Cycle Enzymopathies and Its Role as a Harbinger of Hyperammonemic Coma in PEDIATRIC RESEARCH
  • 1978-04 507 CORRECTION OF HYEPAMMONEMIA IN ARGININOSUCCINIC ACID EMIA BY STIMULATING ARGNINOSUCCINIC ACID (ASA) SYNTHESIS in PEDIATRIC RESEARCH
  • 1978-04 542 DIETARY THERAPY OF ORNITHINE TRANSCARBAMYLASE (OTC) DEFICIENCY in PEDIATRIC RESEARCH
  • 1978-03 Asymptomatic Hyperammonemia in Low Birthweight Infants in PEDIATRIC RESEARCH
  • 1977-04 HYPERAHMONEMIA IN PREMATURE INFANTS in PEDIATRIC RESEARCH
  • 1977-04 THE MECHANISM OF HYPERAMMONEMIA IN CITRULLINEMIA in PEDIATRIC RESEARCH
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