O. Harding, Cary: search on Z-Library

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1

State-of-the-Art 2019 on Gene therapy for Phenylketonuria

Grisch-Chan, Hiu Man, Schwank, Gerald, Harding, Cary O, Thony, Beat

Journal:

Human Gene Therapy

Year:

2019

Language:

english

File:

PDF, 386 KB

english, 2019

2

Aluminum Toxicity

Gilbert-Barness, Enid, Barness, Lewis A., Wolff, Jon, Harding, Cary

Journal:

Archives of Pediatrics and Adolescent Medicine

Year:

1998

Language:

english

File:

PDF, 146 KB

english, 1998

3

Long-term survival in typical thanatophoric dysplasia type 1

Baker, Kristin M., Olson, David S., Harding, Cary O., Pauli, Richard M.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 2.07 MB

english, 1997

4

Functional methionine synthase deficiency due to cblG disorder: A report of two patients and a review

Harding, Cary O., Arnold, Georgianne, Barness, Lewis A., Wolff, Jon A., Rosenblatt, David S.

Journal:

American Journal of Medical Genetics

Year:

1997

Language:

english

File:

PDF, 71 KB

english, 1997

5

Advances and challenges in phenylketonuria

Cary O. Harding, Nenad Blau

Journal:

Journal of Inherited Metabolic Disease

Year:

2010

Language:

english

File:

PDF, 101 KB

english, 2010

6

Prevalence and Distribution of the c.1436C→T Sequence Variant of Carnitine Palmitoyltransferase 1A among Alaska Native Infants

Bradford D. Gessner, Melanie B. Gillingham, Monique A. Johnson, C. Sue Richards, William E. Lambert, David Sesser, Leanne C. Rien, Cheryl A. Hermerath, Michael R. Skeels, Stephanie Birch, Cary O. Hard

Journal:

The Journal of Pediatrics

Year:

2011

Language:

english

File:

PDF, 546 KB

english, 2011

7

Normal vitamin D levels and bone mineral density among children with inborn errors of metabolism consuming medical food–based diets

Geiger, Katie E., Koeller, David M., Harding, Cary O., Huntington, Kathleen L., Gillingham, Melanie B.

Journal:

Nutrition Research

Year:

2016

Language:

english

File:

PDF, 482 KB

english, 2016

8

Tetrahydrobiopterin treatment reduces brain L-Phe but only partially improves serotonin in hyperphenylalaninemic ENU1/2 mice

Scherer, Tanja, Allegri, Gabriella, Sarkissian, Christineh N., Ying, Ming, Grisch-Chan, Hiu Man, Rassi, Anahita, Winn, Shelley R., Harding, Cary O., Martinez, Aurora, Thöny, Beat

Journal:

Journal of Inherited Metabolic Disease

Year:

2018

Language:

english

File:

PDF, 815 KB

english, 2018

9

Higher Dietary Protein Intake preserves lean body mass, lowers liver lipid deposition, and maintains metabolic control in participants with long‐chain fatty acid oxidation disorders

Gillingham, Melanie B., Elizondo, Gabriela, Behrend, Annie, Matern, Dietrich, Schoeller, Dale A., Harding, Cary O., Purnell, Jonathan Q.

Journal:

Journal of Inherited Metabolic Disease

Year:

2019

Language:

english

File:

PDF, 2.33 MB

english, 2019

10

Incidence of tuberous sclerosis in patients with cardiac rhabdomyoma

Cary O. Harding, Roberta A. Pagon

Journal:

American Journal of Medical Genetics Part A

Year:

1990

Language:

english

File:

PDF, 502 KB

english, 1990

11

Reply to Drs. Webb and Osborne on Incidence of Tuberous Sclerosis in Patients With Cardiac Rhabdomyoma

Cary O. Harding, Roberta A. Pagon

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 80 KB

english, 1992

12

Case reports of successful pregnancy in women with maple syrup urine disease and propionic acidemia

Sandra C. Van Calcar, Cary O. Harding, Susan R. Davidson, Lewis A. Barness, Jon A. Wolff

Journal:

American Journal of Medical Genetics Part A

Year:

1992

Language:

english

File:

PDF, 578 KB

english, 1992

13

Expression of phenylalanine hydroxylase (PAH) in erythrogenic bone marrow does not correct hyperphenylalaninemia in Pahenu2 mice

Cary O. Harding, Mark Neff, Kelly Jones, Krzysztof Wild, Jon A. Wolff

Journal:

The Journal of Gene Medicine

Year:

2003

Language:

english

File:

PDF, 169 KB

english, 2003

14

Undergraduate course in environmental design and manufacturing

Andrew S. Borchers, Trevor Harding, Terri Lynch-Caris, Benjamin Redekop, Craig Hof, Jackie El-Sayed, Daryl Doyle

Journal:

Journal of Manufacturing Systems

Year:

2005

Language:

english

File:

PDF, 633 KB

english, 2005

15

Respiratory complications in children with spondyloepiphyseal dysplasia congenita

Cary O. Harding, Christopher G. Green, William H. Perloff, Richard M. Pauli

Journal:

Pediatric Pulmonology

Year:

1990

Language:

english

File:

PDF, 620 KB

english, 1990

16

Therapeutic liver repopulation for phenylketonuria

Cary O. Harding, K. M. Gibson

Journal:

Journal of Inherited Metabolic Disease

Year:

2010

Language:

english

File:

PDF, 153 KB

english, 2010

17

Intracerebral accumulation of glutaric and 3-hydroxyglutaric acids secondary to limited flux across the blood–brain barrier constitute a biochemical risk factor for neurodegeneration in glutaryl-CoA dehydrogenase deficiency

Sven W. Sauer, Jürgen G. Okun, Gert Fricker, Anne Mahringer, Ines Müller, Linda R. Crnic, Chris Mühlhausen, Georg F. Hoffmann, Friederike Hörster, Stephen I. Goodman, Cary O. Harding, David M. Koeller

Journal:

Journal of Neurochemistry

Year:

2006

Language:

english

File:

PDF, 432 KB

english, 2006

18

‘Mommy, why can’t I have a hamburger like the other kids?’

O Harding, Cary

Journal:

Year:

2000

Language:

english

File:

PDF, 72 KB

english, 2000

19

Potential for Misdiagnosis Due to Lack of Metabolic Derangement in Combined Methylmalonic Aciduria/Hyperhomocysteinemia (cblC) in the Neonate

Harding, Cary O, Pillers, De-Ann M, Steiner, Robert D, Bottiglieri, Teodoro, Rosenblatt, David S, Debley, Jason, Michael Gibson, K

Journal:

Journal of Perinatology

Year:

2003

Language:

english

File:

PDF, 71 KB

english, 2003

20

L-2-oxothiazolidine-4-carboxylate supplementation in murine γ-GT deficiency

Patrice Held, Cary O. Harding

Journal:

Free Radical Biology and Medicine

Year:

2003

Language:

english

File:

PDF, 86 KB

english, 2003

21

The Mouse Mutation Sarcosinemia (sar) Maps to Chromosome 2 in a Region Homologous to Human 9q33–q34

Ana Lúcia Bueno Brunialti, Cary O. Harding, Jon A. Wolff, Jean-Louis Guénet

Journal:

Year:

1996

Language:

english

File:

PDF, 80 KB

english, 1996

22

The fate of intravenously administered tetrahydrobiopterin and its implications for heterologous gene therapy of phenylketonuria

Cary O Harding, Mark Neff, Krzysztof Wild, Kelly Jones, Lina Elzaouk, Beat Thöny, Sheldon Milstien

Journal:

Molecular Genetics and Metabolism

Year:

2004

Language:

english

File:

PDF, 186 KB

english, 2004

23

State-of-the-art 2003 on PKU gene therapy

Zhaobing Ding, Cary O Harding, Beat Thöny

Journal:

Molecular Genetics and Metabolism

Year:

2004

Language:

english

File:

PDF, 114 KB

english, 2004

24

Myoadenylate deaminase deficiency caused by alternative splicing due to a novel intronic mutation in the AMPD1 gene

Paul J. Isackson, Heather Bujnicki, Cary O. Harding, Georgirene D. Vladutiu

Journal:

Molecular Genetics and Metabolism

Year:

2005

Language:

english

File:

PDF, 255 KB

english, 2005

25

Effect of optimal dietary therapy upon visual function in children with long-chain 3-hydroxyacyl CoA dehydrogenase and trifunctional protein deficiency

Melanie B. Gillingham, Richard G. Weleber, Martha Neuringer, William E. Connor, Monte Mills, Sandy van Calcar, James ver Hoeve, Jon Wolff, Cary O. Harding

Journal:

Molecular Genetics and Metabolism

Year:

2005

Language:

english

File:

PDF, 354 KB

english, 2005

26

Metabolic control during exercise with and without medium-chain triglycerides (MCT) in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency

Melanie B. Gillingham, Bradley Scott, Diane Elliott, Cary O. Harding

Journal:

Molecular Genetics and Metabolism

Year:

2006

Language:

english

File:

PDF, 237 KB

english, 2006

27

Effects of higher dietary protein intake on energy balance and metabolic control in children with long-chain 3-hydroxy acyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiency

Melanie B. Gillingham, Jonathan Q. Purnell, Julia Jordan, Diane Stadler, Andrea M. Haqq, Cary O. Harding

Journal:

Molecular Genetics and Metabolism

Year:

2007

Language:

english

File:

PDF, 285 KB

english, 2007

28

A Delphi clinical practice protocol for the management of very long chain acyl-CoA dehydrogenase deficiency

Georgianne L. Arnold, Johan Van Hove, Debra Freedenberg, Arnold Strauss, Nicola Longo, Barbara Burton, Cheryl Garganta, Can Ficicioglu, Stephen Cederbaum, Cary Harding, Richard G. Boles, Dietrich Mate

Journal:

Molecular Genetics and Metabolism

Year:

2009

Language:

english

File:

PDF, 171 KB

english, 2009

29

Up to date knowledge on different treatment strategies for phenylketonuria

Amaya Bélanger-Quintana, Alberto Burlina, Cary O. Harding, Ania C. Muntau

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 304 KB

english, 2011

30

Hepatocytes from wild-type or heterozygous donors are equally effective in achieving successful therapeutic liver repopulation in murine phenylketonuria (PKU)

Kelly J. Hamman, Shelley R. Winn, Cary O. Harding

Journal:

Molecular Genetics and Metabolism

Year:

2011

Language:

english

File:

PDF, 399 KB

english, 2011

31

Substrate oxidation and cardiac performance during exercise in disorders of long chain fatty acid oxidation

Annie M. Behrend, Cary O. Harding, James D. Shoemaker, Dietrich Matern, David J. Sahn, Diane L. Elliot, Melanie B. Gillingham

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 469 KB

english, 2012

32

Observations regarding retinopathy in mitochondrial trifunctional protein deficiencies

Autumn L. Fletcher, Mark E. Pennesi, Cary O. Harding, Richard G. Weleber, Melanie B. Gillingham

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 750 KB

english, 2012

33

Hand it to the skin in Costello syndrome

Angela Lin, Cary Harding, Michael Silberbach

Journal:

The Journal of Pediatrics

Year:

2004

Language:

english

File:

PDF, 84 KB

english, 2004

34

Leigh syndrome in an infant resulting from mitochondrial DNA depletion

Michael J Absalon, Cary O Harding, Daniel R Fain, Lei Li, Kenneth J Mack

Journal:

Pediatric Neurology

Year:

2001

Language:

english

File:

PDF, 146 KB

english, 2001

35

Optimal dietary therapy of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency

Melanie B Gillingham, William E Connor, Dietrich Matern, Piero Rinaldo, Terry Burlingame, Kaatje Meeuws, Cary O Harding

Journal:

Molecular Genetics and Metabolism

Year:

2003

Language:

english

File:

PDF, 248 KB

english, 2003

36

Wide-band aerials and transmission lines for 20 to 85 Mc/s

Lutkin, F.E., Cary, R.H.J., Harding, G.N.

Journal:

Journal of the Institution of Electrical Engineers - Part IIIA: Radiolocation

Year:

1946

Language:

english

File:

PDF, 913 KB

english, 1946

37

Pharmacologic inhibition of L-tyrosine degradation ameliorates cerebral dopamine deficiency in murine phenylketonuria (PKU)

Harding, Cary O., Winn, Shelley R., Gibson, K. Michael, Arning, Erland, Bottiglieri, Teodoro, Grompe, Markus

Journal:

Journal of Inherited Metabolic Disease

Year:

2014

Language:

english

File:

PDF, 590 KB

english, 2014

38

Treatment of phenylketonuria using minicircle-based naked-DNA gene transfer to murine liver

Viecelli, Hiu Man, Harbottle, Richard P., Wong, Suet Ping, Schlegel, Andrea, Chuah, Marinee K., VandenDriessche, Thierry, Harding, Cary O., Thöny, Beat

Journal:

Year:

2014

Language:

english

File:

PDF, 1.89 MB

english, 2014

39

Use of propofol for short duration procedures in children with long chain 3-hydroxyacyl-CoA dehydrogenase (LCHAD) or trifunctional protein (TFP) deficiencies

Martin, Julie M., Gillingham, Melanie B., Harding, Cary O.

Journal:

Molecular Genetics and Metabolism

Year:

2014

Language:

english

File:

PDF, 191 KB

english, 2014

40

Infants suspected to have very-long chain acyl-CoA dehydrogenase deficiency from newborn screening

Merritt, J. Lawrence, Vedal, Sverre, Abdenur, Jose E., Au, Sylvia M., Barshop, Bruce A., Feuchtbaum, Lisa, Harding, Cary O., Hermerath, Cheryl, Lorey, Fred, Sesser, David E., Thompson, John D., Yu, Ar

Journal:

Molecular Genetics and Metabolism

Year:

2014

Language:

english

File:

PDF, 742 KB

english, 2014

41

Fumarylacetoacetate hydrolase deficient pigs are a novel large animal model of metabolic liver disease

Hickey, Raymond D., Mao, Shennen A., Glorioso, Jaime, Lillegard, Joseph B., Fisher, James E., Amiot, Bruce, Rinaldo, Piero, Harding, Cary O., Marler, Ronald, Finegold, Milton J., Grompe, Markus, Nyber

Journal:

Stem Cell Research

Year:

2014

Language:

english

File:

PDF, 1.59 MB

english, 2014

42

Ours Editeur

Hickey, Raymond D., Mao, Shennen A., Glorioso, Jaime, Lillegard, Joseph B., Fisher, James E., Amiot, Bruce, Rinaldo, Piero, Harding, Cary O., Marler, Ronald, Finegold, Milton J., Grompe, Markus, Nyber

Journal:

Revue de Pneumologie Clinique

Year:

2010

Language:

french

File:

PDF, 67 KB

french, 2010

43

Single-dose, subcutaneous recombinant phenylalanine ammonia lyase conjugated with polyethylene glycol in adult patients with phenylketonuria: an open-label, multicentre, phase 1 dose-escalation trial

Longo, Nicola, Harding, Cary O, Burton, Barbara K, Grange, Dorothy K, Vockley, Jerry, Wasserstein, Melissa, Rice, Gregory M, Dorenbaum, Alejandro, Neuenburg, Jutta K, Musson, Donald G, Gu, Zhonghua, S

Journal:

Year:

2014

Language:

english

File:

PDF, 314 KB

english, 2014

44

Ammonia Control in Children Ages 2 Months through 5 Years with Urea Cycle Disorders: Comparison of Sodium Phenylbutyrate and Glycerol Phenylbutyrate

Smith, Wendy, Diaz, George A., Lichter-Konecki, Uta, Berry, Susan A., Harding, Cary O., McCandless, Shawn E., LeMons, Cindy, Mauney, Joe, Dickinson, Klara, Coakley, Dion F., Moors, Tristen, Mokhtarani

Journal:

The Journal of Pediatrics

Year:

2013

Language:

english

File:

PDF, 415 KB

english, 2013

45

Molecular Basis of Two-Exon Skipping (Exons 12 and 13) by c.1248+5g>a in OXCT1 Gene: Study on Intermediates of OXCT1 Transcripts in Fibroblasts

Hori, Tomohiro, Fukao, Toshiyuki, Murase, Keiko, Sakaguchi, Naomi, Harding, Cary O., Kondo, Naomi

Journal:

Year:

2013

Language:

english

File:

PDF, 443 KB

english, 2013

46

Comparison of Adeno-Associated Virus Pseudotype 1, 2, and 8 Vectors Administered by Intramuscular Injection in the Treatment of Murine Phenylketonuria

Rebuffat, Alexandre, Harding, Cary O., Ding, Zhaobing, Thöny, Beat

Journal:

Human Gene Therapy

Year:

2010

Language:

english

File:

PDF, 2.15 MB

english, 2010

47

Seeking a Cure for the Royal Pain

Harding, Cary O.

Journal:

Human Gene Therapy

Year:

2013

Language:

english

File:

PDF, 48 KB

english, 2013

48

219. Persistent Correction of Hyperphenylalaninemia Following Liver-Directed, rAAV2/8-Mediated Gene Therapy for Murine Phenylketonuria (PKU)

Harding, Cary O., Gillingham, Melanie B., Daghighi, Elizabeth, Bird, Andrew, Koeberl, Dwight D.

Journal:

Molecular Therapy

Year:

2006

Language:

english

File:

PDF, 83 KB

english, 2006

49

A Sensitive Assay System To Test Antisense Oligonucleotides for Splice Suppression Therapy in the Mouse Liver

Gallego-Villar, Lorena, Viecelli, Hiu Man, Pérez, Belén, Harding, Cary O, Ugarte, Magdalena, Thöny, Beat, Desviat, Lourdes R

Journal:

Molecular Therapy — Nucleic Acids

Year:

2014

Language:

english

File:

PDF, 1.64 MB

english, 2014

50

404. Therapeutic Correction of PKU in a Mouse Model by Ectopic Expression of PAH and Its BH4- Cofactor Genes in Skeletal Muscle by a Recombinant Triple-Cistronic AAV2-Based Pseudotype 1 Vector

Ding, Zhaobing, O. Harding, Cary, Rebuffat, Alexandre, Elzaouk, Lina, Wolff, Jon A., Thony, Beat

Journal:

Molecular Therapy

Year:

2006

Language:

english

File:

PDF, 95 KB

english, 2006