WHITLEY, CHESTER B.: search on Z-Library

The world's largest scientific articles store. 70,000,000+ articles for free.

Don't use scam websites

1

Placebo Controlled Trial Evaluating Gabapentin for the Treatment of Small Fiber Neuropathic Pain in Patients with Fabry Disease

Jonica Hazaert, Kyle D. Rudser, Jeanine R. Utz, Chester B. Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 57 KB

english, 2012

2

A novel Blind Start study design to investigate vestronidase alfa for mucopolysaccharidosis VII, an ultra-rare genetic disease

Harmatz, Paul, Whitley, Chester B., Wang, Raymond Y., Bauer, Mislen, Song, Wenjie, Haller, Christine, Kakkis, Emil

Journal:

Molecular Genetics and Metabolism

Year:

2018

Language:

english

File:

PDF, 307 KB

english, 2018

3

Correction of both Tay-Sachs and Sandhoff diseases with the PS gene editing system

Ou, Li, Przybilla, Michael, TÄbÄran, Alexandru-Flaviu, Overn, Paula, O'Sullivan, Gerard, Jiang, Xuntian, Sidhu, Rohini, Kell, Pamela, Ory, Daniel, Whitley, Chester B.

Journal:

Molecular Genetics and Metabolism

Year:

2020

File:

PDF, 323 KB

2020

4

130. Neuropsychological outcomes in Hurler syndrome: 7–20 years post-hematopoietic stem cell transplantion

Elsa Shapiro, Kendra Bjoraker, Evren Guler, Kathleen Delaney, Lawrence Charnas, Jakub Tolar, Chester Whitley, Kathleen Thomas

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 53 KB

english, 2009

5

Impact of growth hormone on changes in height, bone mineral density, lean body mass, and body fat over 1–2 years in children with Hurler or Hunter syndrome

Polgreen, Lynda, Miller, Bradley S., Thomas, William, Whitley, Chester B.

Journal:

Molecular Genetics and Metabolism

Year:

2013

Language:

english

File:

PDF, 76 KB

english, 2013

6

Increased substrate concentration boosts enzyme activity levels of fluorometric α-l-iduronidase enzyme activity assay

Herzog, Tyler, Ou, Li, Whitley, Chester

Journal:

Molecular Genetics and Metabolism

Year:

2013

Language:

english

File:

PDF, 65 KB

english, 2013

7

Phenotype prediction for mucopolysaccharidosis type I by in silico analysis

Ou, Li, Przybilla, Michael J., Whitley, Chester B.

Journal:

Orphanet Journal of Rare Diseases

Year:

2017

Language:

english

File:

PDF, 1.65 MB

english, 2017

8

Beneath the floor: re-analysis of neurodevelopmental outcomes in untreated Hurler syndrome

Shapiro, Elsa G., Whitley, Chester B., Eisengart, Julie B.

Journal:

Orphanet Journal of Rare Diseases

Year:

2018

Language:

english

File:

PDF, 812 KB

english, 2018

9

Clinical and biochemical heterogeneity in females of a large pedigree with ornithine transcarbamylase deficiency due to the R141Q mutation

Ahrens, Mary J., Berry, Susan A., Whitley, Chester B., Markowitz, Dorothy J., Plante, Robert J., Tuchman, Mendel

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 395 KB

english, 1996

10

Closed hollow-fiber bioreactor: a new approach to retroviral vector production

Dao Pan, Chester B. Whitley

Journal:

The Journal of Gene Medicine

Year:

1999

Language:

english

File:

PDF, 135 KB

english, 1999

11

Fibrochondrogenesis: Lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology

Dr. Chester B. Whitley, Leonard O. Langer Jr., Janice Ophoven, Enid F. Gilbert, Claudette H. Gonzalez, Mark Mammel, Michael Coleman, Sergio Rosemberg, Consuelo J. Rodriques, Richard Sibley, William A.

Journal:

American Journal of Medical Genetics Part A

Year:

1984

Language:

english

File:

PDF, 1.02 MB

english, 1984

12

De la chapelle dysplasia

Chester B. Whitley, Barbara A. Burke, Gustav Granroth, Robert J. Gorlin, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1986

Language:

english

File:

PDF, 848 KB

english, 1986

13

A nonpathologic allele (IW) for low α-L-iduronidase enzyme activity vis-a-vis prenatal diagnosis of Hurler syndrome

Chester B. Whitley, Robert J. Gorlin, William Krivit, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 606 KB

english, 1987

14

Direct hyperbilirubinemia and hepatic fibrosis: A new presentation of Jeune syndrome (asphyxiating thoracic dystrophy)

Dr. Chester B. Whitley, Sarah Jane Schwarzenberg, Barbara A. Burke, Deborah K. Freese, Robert J. Gorlin, John M. Opitz, Jay Bernstein

Journal:

American Journal of Medical Genetics Part A

Year:

1987

Language:

english

File:

PDF, 587 KB

english, 1987

15

First International Congress on mucopolysaccharidosis and related diseases - 70 years of research, university of Minnesota, Minneapolis, May 20–23, 1988

Chester B. Whitley, John M. Opitz, James F. Reynolds

Journal:

American Journal of Medical Genetics Part A

Year:

1989

Language:

english

File:

PDF, 183 KB

english, 1989

16

Adams-Oliver syndrome revisited

Chester B. Whitley, Robert J. Gorlin

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 762 KB

english, 1991

17

Long-term outcome of Hurler syndrome following bone marrow transplantation

Chester B. Whitley, Kumar G. Belani, Pi-Nian Chang, C. Gail Summers, Bruce R. Blazar, Michael Y. Tsai, Richard E. Latchaw, Norma K. C. Ramsay, John H. Kersey

Journal:

American Journal of Medical Genetics Part A

Year:

1993

Language:

english

File:

PDF, 1.04 MB

english, 1993

18

Caveat to genotype–phenotype correlation in mucopolysaccharidosis type II: Discordant clinical severity of R468W and R468Q mutations of the iduronate-2-sulfatase gene

Chester B. Whitley, Rose Ann Anderson, Elena L. Aronovich, Paul L. Crotty, Kwame Anyane-Yeboa, Donna Russo, Dorothy Warburton

Journal:

Year:

1993

Language:

english

File:

PDF, 259 KB

english, 1993

19

Prolonged expression of a lysosomal enzyme in mouse liver after Sleeping Beauty transposon-mediated gene delivery: implications for non-viral gene therapy of mucopolysaccharidoses

Elena L. Aronovich, Jason B. Bell, Lalitha R. Belur, Roland Gunther, Brenda Koniar, David C. C. Erickson, Patricia A. Schachern, Ilze Matise, R. Scott McIvor, Chester B. Whitley, Perry B. Hackett

Journal:

The Journal of Gene Medicine

Year:

2007

Language:

english

File:

PDF, 1.41 MB

english, 2007

20

Construction of a high efficiency retroviral vector for gene therapy of Hunter's syndrome

Youngtae Hong, Seung Shin Yu, Jong-Mook Kim, Karim Lee, Young Soon Na, Chester B. Whitley, Yoshikazu Sugimoto, Sunyoung Kim

Journal:

The Journal of Gene Medicine

Year:

2003

Language:

english

File:

PDF, 216 KB

english, 2003

21

Excision of Sleeping Beauty transposons: parameters and applications to gene therapy

Geyi Liu, Elena L. Aronovich, Zongbin Cui, Chester B. Whitley, Perry B. Hackett

Journal:

The Journal of Gene Medicine

Year:

2004

Language:

english

File:

PDF, 340 KB

english, 2004

22

Improved gene transfer and normalized enzyme levels in primitive hematopoietic progenitors from patients with mucopolysaccharidosis type I using a bioreactor

Dao Pan, David F. Stroncek, Chester B. Whitley

Journal:

The Journal of Gene Medicine

Year:

2004

Language:

english

File:

PDF, 245 KB

english, 2004

23

Direct gene transfer to the CNS prevents emergence of neurologic disease in a murine model of mucopolysaccharidosis type I

Daniel A. Wolf, Andrew W. Lenander, Zhenhong Nan, Lalitha R. Belur, Chester B. Whitley, Pankaj Gupta, Walter C. Low, R. Scott McIvor

Journal:

Neurobiology of Disease

Year:

2011

Language:

english

File:

PDF, 2.03 MB

english, 2011

24

Retroviral transduction of peripheral blood leukocytes in a hollow- fiber bioreactor

Raji Shankar, Chester B. Whitley, Dao Pan, Scott Burger, Jeffrey McCullough, David Stroncek

Journal:

Transfusion (Wiley)

Year:

1997

Language:

english

File:

PDF, 535 KB

english, 1997

25

Retroviral transduction and expansion of peripheral blood lymphocytes for the treatment of mucopolysaccharidosis type II, Hunter's syndrome

David F. Stroncek, Allison Hubel, Raji A. Shankar, Scott R. Burger, Dao Pan, Jeffrey McCullough, Chester B. Whitley

Journal:

Transfusion (Wiley)

Year:

1999

Language:

english

File:

PDF, 744 KB

english, 1999

26

Assessment of iduronate-2-sulfatase mRNA expression in Hunter syndrome (mucopolysaccharidosis type II)

Paul L. Crotty, Chester B. Whitley

Journal:

Year:

1992

Language:

english

File:

PDF, 420 KB

english, 1992

27

A preliminary report on dopamine system reactivity in PKU: acute effects of haloperidol on neuropsychological, physiological, and neuroendocrine functions

Monica Luciana, Karen L. Hanson, Chester B. Whitley

Journal:

Psychopharmacology

Year:

2004

Language:

english

File:

PDF, 150 KB

english, 2004

28

Syringomyelia in mucopolysaccharidosis type VI (Maroteaux-Lamy syndrome): imaging findings following bone marrow transplantation

S. H. Hite, William Krivit, Stephen J. Haines, Chester B. Whitley

Journal:

Pediatric Radiology

Year:

1997

Language:

english

File:

PDF, 331 KB

english, 1997

29

Pre-stem cell transplantation enzyme replacement therapy in Hurler syndrome does not lead to significant antibody formation or delayed recovery of the endogenous enzyme post-transplant: A case report

Sandeep Soni, Monica Hente, Nancy Breslin, Joseph Hersh, Chester Whitley, Alexandra Cheerva, Salvatore Bertolone

Journal:

Pediatric Transplantation

Year:

2007

Language:

english

File:

PDF, 510 KB

english, 2007

30

Evaluation of coronary artery disease in the Hurler syndrome by angiography

Elizabeth A. Braunlin, David W. Hunter, William Krivit, Barbara A. Burke, Peter S. Hesslein, Priscilla T. Porter, Chester B. Whitley

Journal:

The American Journal of Cardiology

Year:

1992

Language:

english

File:

PDF, 2.25 MB

english, 1992

31

Cardiac Findings After Enzyme Replacement Therapy for Mucopolysaccharidosis Type I

Elizabeth A. Braunlin, James M. Berry, Chester B. Whitley

Journal:

The American Journal of Cardiology

Year:

2006

Language:

english

File:

PDF, 85 KB

english, 2006

32

Canine Heparan Sulfate Sulfamidase and the Molecular Pathology Underlying Sanfilippo Syndrome Type A in Dachshunds

Elena L. Aronovich, K.Paige Carmichael, Hiroki Morizono, Ioannis G. Koutlas, Minerva Deanching, George Hoganson, Andrea Fischer, Chester B. Whitley

Journal:

Year:

2000

Language:

english

File:

PDF, 274 KB

english, 2000

33

Molecular Basis of Mucopolysaccharidosis Type IIIB in Emu (Dromaius novaehollandiae): An Avian Model of Sanfilippo Syndrome Type B

Elena L. Aronovich, Jade M. Johnston, Ping Wang, Urs Giger, Chester B. Whitley

Journal:

Year:

2001

Language:

english

File:

PDF, 655 KB

english, 2001

34

“Supercharged Cells” for Delivery of Recombinant Human Iduronate-2-Sulfatase

Dao Pan, Jon J. Jonsson, Stephen E. Braun, R.Scott McIvor, Chester B. Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2000

Language:

english

File:

PDF, 166 KB

english, 2000

35

Urinary Glycosaminoglycan Excretion Quantified by an Automated Semimicro Method in Specimens Conveniently Transported from Around the Globe

Chester B. Whitley, Richard C. Spielmann, Gerrard Herro, Suzanne Severson Teragawa

Journal:

Molecular Genetics and Metabolism

Year:

2002

Language:

english

File:

PDF, 165 KB

english, 2002

36

Children with mucopolysaccharidosis: Perioperative care, morbidity, mortality, and new findings

Kumar G. Belani, William Krivit, Becky L.M. Carpenter, Elizabeth Braunlin, Joseph J. Buckley, Ji-Chia Liao, Thomas Floyd, Arnold S. Leonard, C. Gail Summers, Samuel Levine, Chester B. Whitley

Journal:

Journal of Pediatric Surgery

Year:

1993

Language:

english

File:

PDF, 917 KB

english, 1993

37

Age-related functional and histopathological changes of the ear in the MPS I mouse

Patricia A. Schachern, Sebahattin Cureoglu, Vladimir Tsuprun, Michael M. Paparella, Chester B. Whitley

Journal:

International Journal of Pediatric Otorhinolaryngology

Year:

2007

Language:

english

File:

PDF, 1.95 MB

english, 2007

38

Enzyme replacement therapy in mucopolysaccharidosis VI (Maroteaux-Lamy syndrome)

Paul Harmatz, Chester B Whitley, Lewis Waber, Ray Pais, Robert Steiner, Barbara Plecko, Paige Kaplan, Julie Simon, Ellen Butensky, John J Hopwood

Journal:

The Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 167 KB

english, 2004

39

High rate of postoperative mortality in patients with mucopolysaccharidosis I: findings from the MPS I Registry

Pamela Arn, Chester Whitley, J. Edmond Wraith, H. Warner Webb, Lisa Underhill, Lakshmi Rangachari, Gerald F. Cox

Journal:

Journal of Pediatric Surgery

Year:

2012

Language:

english

File:

PDF, 140 KB

english, 2012

40

11 Adeno-associated virus vector-mediated gene therapy in a murine model of mucopolysaccharidosis type I

Lalitha Belur, Zachary deMorest, Chester B. Whitley, Walter C. Low, R. Scott McIvor

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 58 KB

english, 2007

41

31 Hippocampal functions in MPS I: A pilot study of memory encoding and visual spatial function

Elsa Shapiro, Kendra Bjoraker, Kate Delaney, Chester Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 60 KB

english, 2007

42

100 Age-related functional and histopathological changes of the ear in the MPS I mouse

Patricia Schachern, Sebahattin Cureoglu, Vladimir Tsuprun, Michael Paparella, Chester Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 58 KB

english, 2007

43

40 Endocrine abnormalities in patients with mucopolysaccharidoses

Lynda Polgreen, Melissa Plog, Paul Orchard, Bradley Miller, Anna Petryk, Chester B. Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 56 KB

english, 2007

44

11. A natural history study of hexosaminidase deficiency

Kendra Bjoraker, Colleen Doyen, Chester B. Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 55 KB

english, 2008

45

85 Molecular basis for unusually low alpha-l-iduronidase activity in normal individuals

Arthur T. Johnson, Sherri L. Sandberg, Irwin Schaeffer, Jennifer Stein, Chester B. Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 43 KB

english, 2007

46

4. Sleeping Beauty transposon-mediated long-term α-l-iduronidase expression and correction of lysosomal pathology in NOD/SCID mice with MPS I

Elena Aronovich, Jason Bell, Lalitha Belur, Rolund Gunther, Koniar Brenda, Shaukat Kahn, Patricia Schachern, Robert Ehlenfeldt, Pankaj Gupta, Cathy Carlson, Chester Whitley, R. Scott McIvor, Perry Hac

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 44 KB

english, 2008

47

89. Neuropsychological function and neuroimaging in severe and attenuated mucopolysaccharidosis

Elsa Shapiro, Kathleen Thomas, Kathleen Delaney, Kendra Bjoraker, Whitley Chester, Charnas Lawrence

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 42 KB

english, 2008

48

8. Adeno-associated virus gene therapy for Tay-Sachs disease

Lee Bera, Chester Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 43 KB

english, 2008

49

70. Gene therapy for lysosomal storage disorders

R. Scott McIvor, Walter C. Low, Perry B. Hackett, Chester B. Whitley

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 44 KB

english, 2008

50

69. Gene therapy of mucopolysaccharidosis type I: Intraventricular administration of adeno-associated virus vector transducing the human alpha-l-iduronidase gene in a murine model of the disease

R. Scott McIvor, Daniel A. Wolf, Zhenhong Nan, Mayra Quito, Kelly Podetz-Pedersen, Chester B. Whitley, Walter C. Low, Lalitha R. Belur

Journal:

Molecular Genetics and Metabolism

Year:

2008

Language:

english

File:

PDF, 41 KB

english, 2008