M. L. Batshaw: search on Z-Library

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1

Down Syndrome

Hayes, Adadot, Batshaw, Mark L.

Journal:

Pediatric Clinics of North America

Year:

1993

Language:

english

File:

PDF, 1.34 MB

english, 1993

2

Hyperammonemia

Mark L. Batshaw

Journal:

Current Problems in Pediatric and Adolescent Health Care

Year:

1984

Language:

english

File:

PDF, 5.19 MB

english, 1984

3

A dual AAV system enables the Cas9-mediated correction of a metabolic liver disease in newborn mice

Yang, Yang, Wang, Lili, Bell, Peter, McMenamin, Deirdre, He, Zhenning, White, John, Yu, Hongwei, Xu, Chenyu, Morizono, Hiroki, Musunuru, Kiran, Batshaw, Mark L, Wilson, James M

Journal:

Nature Biotechnology

Year:

2016

Language:

english

File:

PDF, 1.73 MB

english, 2016

4

Inborn errors of urea synthesis

Dr. Mark L. Batshaw

Journal:

Annals of Neurology

Year:

1994

Language:

english

File:

PDF, 888 KB

english, 1994

5

Inherited hyperammonemia: An algorithm for diagnosis

Mark L. Batshaw

Journal:

Year:

1987

Language:

english

File:

PDF, 257 KB

english, 1987

6

Clinical research for rare disease: Opportunities, challenges, and solutions

Robert C. Griggs, Mark Batshaw, Mary Dunkle, Rashmi Gopal-Srivastava, Edward Kaye, Jeffrey Krischer, Tan Nguyen, Kathleen Paulus, Peter A. Merkel

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 223 KB

english, 2009

7

Amino acid acylation: a mechanism of nitrogen excretion in inborn errors of urea synthesis

Brusilow, S, Tinker, J, Batshaw, M.

Journal:

Year:

1980

Language:

english

File:

PDF, 1015 KB

english, 1980

8

Improving long term outcomes in urea cycle disorders-report from the Urea Cycle Disorders Consortium

Waisbren, Susan E., Gropman, Andrea L., Batshaw, Mark L.

Journal:

Journal of Inherited Metabolic Disease

Year:

2016

Language:

english

File:

PDF, 1.61 MB

english, 2016

9

Genotype spectrum of ornithine transcarbamylase deficiency: Correlation with the clinical and biochemical phenotype

Beth A. McCullough, Marc Yudkoff, Mark L. Batshaw, James M. Wilson, Steven E. Raper, Mendel Tuchman

Journal:

American Journal of Medical Genetics Part A

Year:

2000

Language:

english

File:

PDF, 205 KB

english, 2000

10

Long-term gene transfer to mouse fetuses with recombinant adenovirus and adeno-associated virus (AAV) vectors

Mitchell, M, Jerebtsova, M, Batshaw, M L, Newman, K, Ye, X

Journal:

Year:

2000

Language:

english

File:

PDF, 862 KB

english, 2000

11

Developing adenoviral-mediated in vivo gene therapy for ornithine transcarbamylase deficiency

S. E. Raper, J. M. Wilson, M. Yudkoff, M. B. Robinson, X. Ye, M. L. Batshaw

Journal:

Journal of Inherited Metabolic Disease

Year:

1998

Language:

english

File:

PDF, 201 KB

english, 1998

12

Neurotransmitter alterations in congenital hyperammonemia

Dr. Michael B. Robinson, Mark L. Batshaw

Journal:

Development Diabilities Research Reviews

Year:

1995

Language:

english

File:

PDF, 933 KB

english, 1995

13

Cognitive Development in Children with Inborn Errors of Urea Synthesis

Michael Msall, Peggy S. Monahan, Natalia Chapanis, Mark L. Batshaw

Journal:

Pediatrics International

Year:

1988

Language:

english

File:

PDF, 717 KB

english, 1988

14

Unsuccessful treatment of phenylketonuria with tyrosine

Mark L. Batshaw, David Valle, Samuel P. Bessman

Journal:

The Journal of Pediatrics

Year:

1981

Language:

english

File:

PDF, 173 KB

english, 1981

15

Treatment of Episodic Hyperammonemia in Children with Inborn Errors of Urea Synthesis

Brusilow, Saul W., Danney, Mark, Waber, Lewis J., Batshaw, Mark, Burton, Barbara, Levitsky, Lynn, Roth, Karl, McKeethren, Carla, Ward, Jewell

Journal:

Boston Medical and Surgical Journal

Year:

1984

Language:

english

File:

PDF, 860 KB

english, 1984

16

Differences in the Human and Mouse Amino-Terminal Leader Peptides of Ornithine Transcarbamylase Affect Mitochondrial Import and Efficacy of Adenoviral Vectors

Ye, Xuehai, Zimmer, Klaus-Peter, Brown, Rebecca, Pabin, Carol, Batshaw, Mark L., Wilson, James M., Robinson, Michael B.

Journal:

Human Gene Therapy

Year:

2001

Language:

english

File:

PDF, 951 KB

english, 2001

17

Behavioral and Neurotransmitter Changes in the Urease-Infused Rat: A Model of Congenital Hyperammonemia

Batshaw, Mark L, Hyman, Susan L, Mellits, E David, Thomas, George H, DeMuro, Richard, Coyle, Joseph T

Journal:

Pediatric Research

Year:

1986

Language:

english

File:

PDF, 655 KB

english, 1986

18

Cerebral Dysfunction in Asymptomatic Carriers of Ornithine Transcarbamylase Deficiency

Batshaw, Mark L., Roan, Yeai, Jung, August L., Rosenberg, Leon A., Brusilow, Saul W.

Journal:

Boston Medical and Surgical Journal

Year:

1980

File:

PDF, 1.82 MB

1980

19

Handbook of Developmental Disabilities

Batshaw, Mark, Dowrick, Peter, Kurtz, Lisa, Levy, Susan

Journal:

Pediatric Physical Therapy

Year:

2000

File:

PDF, 230 KB

2000

20

Mental Retardation

Batshaw, Mark L.

Journal:

Pediatric Clinics of North America

Year:

1993

Language:

english

File:

PDF, 1.53 MB

english, 1993

21

THE MECHANISM OF HYPERAMMONEMIA IN CITRULLINEMIA

Brusilow, Saul, Batshaw, Mark, Robinson, Brian, Sherwood, Geoffrey, Walser, Mackenzie

Journal:

Pediatric Research

Year:

1977

Language:

english

File:

PDF, 143 KB

english, 1977

22

1559 DEPAKENE (VPA) INDUCED HYPERAMMONEMIA (HA)

Batshaw, Mark L, Valle, David, Brusilow, Saul W

Journal:

Pediatric Research

Year:

1981

Language:

english

File:

PDF, 163 KB

english, 1981

23

Overview: Millennium issue

Mark L. Batshaw

Journal:

Development Diabilities Research Reviews

Year:

2001

Language:

english

File:

PDF, 78 KB

english, 2001

24

Prospects for prenatal gene therapy in disorders causing mental retardation

Xuehai Ye, Melanie Mitchell, Kurt Newman, Mark L. Batshaw

Journal:

Development Diabilities Research Reviews

Year:

2001

Language:

english

File:

PDF, 1.19 MB

english, 2001

25

Positron emission tomographic study of D2 dopamine receptor binding and CSF biogenic amine metabolites in rett syndrome

James C. Harris, Dean F. Wong, Henry N. Wagner Jr., Andreas Rett, Sakkubai Naidu, R. F. Dannals, J. M. Links, Mark L. Batshaw, Hugo W. Moser, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 468 KB

english, 1986

26

A case of ornithine transcarbamylase deficiency with rett syndrome manifestations

Susan L. Hyman, Mark L. Batshaw, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 285 KB

english, 1986

27

Metabolic and neuropsychological phenotype in women heterozygous for ornithine transcarbamylase deficiency

Kunsang Gyato, J. Wray, Z. J. Huang, M. Yudkoff, Mark L. Batshaw

Journal:

Annals of Neurology

Year:

2004

Language:

english

File:

PDF, 84 KB

english, 2004

28

Valproate-induced hyperammonemia

Dr. Mark L. Batshaw, Saul W. Brusilow

Journal:

Annals of Neurology

Year:

1982

Language:

english

File:

PDF, 317 KB

english, 1982

29

Basic neurochemistry, ed 4 Edited by George Siegal, Bernald Agranoff, R. W. Albers, and Perry Molinoff New York, Raven, 1988 984 pages, illustrated, $58.50

Mark L. Batshaw

Journal:

Annals of Neurology

Year:

1989

Language:

english

File:

PDF, 131 KB

english, 1989

30

Quinolinic acid in children with congenital hyperammonemia

Mark L. Batshaw, Michael B. Robinson, Keith Hyland, Sina Djali, Melvyn P. Heyes

Journal:

Annals of Neurology

Year:

1993

Language:

english

File:

PDF, 516 KB

english, 1993

31

Treatment of thecbl Bform of methylmalonic acidaemia with adenosylcobalamin

M. L. Batshaw, G. H. Thomas, S. R. Cohen, R. Matalon, M. J. Mahoney

Journal:

Journal of Inherited Metabolic Disease

Year:

1984

Language:

english

File:

PDF, 524 KB

english, 1984

32

Evidence of lack of toxicity of sodium phenylacetate and sodium benzoate in treating urea cycle enzymopathies

Mark L. Batshaw, Saul W. Brusilow

Journal:

Journal of Inherited Metabolic Disease

Year:

1981

Language:

english

File:

PDF, 127 KB

english, 1981

33

Brain Serotonin2 and Serotonin1A Receptors Are Altered in the Congenitally Hyperammonemic Sparse Fur Mouse

Michael B. Robinson, Norifusa J. Anegawa, Eileen Gorry, Ijaz A. Qureshi, Joseph T. Coyle, Irwin Lucki, Mark L. Batshaw

Journal:

Journal of Neurochemistry

Year:

1992

Language:

english

File:

PDF, 753 KB

english, 1992

34

Correction of argininosuccinate synthetase (AS) deficiency in a murine model of citrullinemia with recombinant adenovirus carrying human AS cDNA

Ye, X, Whiteman, B, Jerebtsova, M, Batshaw, M L

Journal:

Year:

2000

Language:

english

File:

PDF, 210 KB

english, 2000

35

Transient depletion of CD4 lymphocyte improves efficacy of repeated administration of recombinant adenovirus in the ornithine transcarbamylase deficient sparse fur mouse

Ye, X, Robinson, M B, Pabin, C, Batshaw, M L, Wilson, J M

Journal:

Year:

2000

Language:

english

File:

PDF, 415 KB

english, 2000

36

In vivo measurement of ureagenesis with stable isotopes

M. Yudkoff, Y. Daikhin, X. Ye, J. M. Wilson, M. L. Batshaw

Journal:

Journal of Inherited Metabolic Disease

Year:

1998

Language:

english

File:

PDF, 180 KB

english, 1998

37

Mental retardation and developmental disabilities: A new journal of research reviews

Mark L. Batshaw

Journal:

Development Diabilities Research Reviews

Year:

1995

Language:

english

File:

PDF, 124 KB

english, 1995

38

Neurotransmitters and mental retardation

John A. Kessler, Mark L. Batshaw

Journal:

Development Diabilities Research Reviews

Year:

1995

Language:

english

File:

PDF, 199 KB

english, 1995

39

Prospects for gene therapy in ornithine carbamoyltransferase deficiency and other urea cycle disorders

Michael B. Robinson, Mark L. Batshaw, Xuehai Ye, James M. Wilson

Journal:

Development Diabilities Research Reviews

Year:

1995

Language:

english

File:

PDF, 1.09 MB

english, 1995

40

The Clinical and Translational Science Institute at Children's National: Improving Health through pediatric Research

Jill Joseph, Mary Purucker, Kolaleh Eskandanian, Mark Batshaw, Mendel Tuchman

Journal:

Clinical and Translational Science

Year:

2012

Language:

english

File:

PDF, 4.00 MB

english, 2012

41

Measuring Return on Investment of an Intensive Faculty Development Program in Medical Education

Patience H. White, Mark L. Batshaw, Edwin K. Zechman Jr., Bernhard L. Wiedermann

Journal:

The Journal of Pediatrics

Year:

2005

Language:

english

File:

PDF, 91 KB

english, 2005

42

Is there life as an investigator after becoming a pediatric department chair?

Robert McCarter, Mark L. Batshaw

Journal:

The Journal of Pediatrics

Year:

2006

Language:

english

File:

PDF, 152 KB

english, 2006

43

Poster Abstract #15: Preliminary Experience With MRS at 3T in Urea Cycle Disorders Detects Altered Metabolism in Partial Ornithine Transcarbamylase Deficiency

Andrea Gropman, Ayichew Hailu, Rebecca Seltzer, Stanley Fricke, John van Meter, Mark Batshaw, Mendel Tuchman

Journal:

Neurotherapeutics

Year:

2007

Language:

english

File:

PDF, 38 KB

english, 2007

44

Center for Neuroscience and Behavioral Medicine: An Innovative Administrative Structure and Possible Paradigm for the Future

Roger J. Packer, Jocelyn Villongco, Mark Batshaw, Peter Holbrook, William Davis Gaillard, Phillip L. Pearl, Steven Weinstein, Edwin Zechman

Journal:

Pediatric Neurology

Year:

2011

Language:

english

File:

PDF, 271 KB

english, 2011

45

Fatal systemic inflammatory response syndrome in a ornithine transcarbamylase deficient patient following adenoviral gene transfer

Steven E Raper, Narendra Chirmule, Frank S Lee, Nelson A Wivel, Adam Bagg, Guang-ping Gao, James M Wilson, Mark L Batshaw

Journal:

Molecular Genetics and Metabolism

Year:

2003

Language:

english

File:

PDF, 317 KB

english, 2003

46

Cognitive outcome in urea cycle disorders

Andrea L Gropman, Mark L Batshaw

Journal:

Molecular Genetics and Metabolism

Year:

2004

Language:

english

File:

PDF, 116 KB

english, 2004

47

1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency

A.L. Gropman, S.T. Fricke, R.R. Seltzer, A. Hailu, A. Adeyemo, A. Sawyer, J. van Meter, W.D. Gaillard, R. McCarter, M. Tuchman, M. Batshaw

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 1.29 MB

english, 2008

48

Alternative pathway or diversion therapy for urea cycle disorders now and in the future

Stephen Cederbaum, Cynthia LeMons, Mark L. Batshaw

Journal:

Molecular Genetics and Metabolism

Year:

2010

Language:

english

File:

PDF, 118 KB

english, 2010

49

Preclinical evaluation of a clinical candidate AAV8 vector for ornithine transcarbamylase (OTC) deficiency reveals functional enzyme from each persisting vector genome

Lili Wang, Hiroki Morizono, Jianping Lin, Peter Bell, David Jones, Deirdre McMenamin, Hongwei Yu, Mark L. Batshaw, James M. Wilson

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 1.27 MB

english, 2012

50

Hepatocellular carcinoma in a research subject with ornithine transcarbamylase deficiency

James M. Wilson, Oleg A. Shchelochkov, Renata C. Gallagher, Mark L. Batshaw

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 150 KB

english, 2012