Dennis W. Bartholomew: search on Z-Library

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1

Docosahexaenoic Acid and Amino Acid Contents in Pasteurized Donor Milk are Low for Preterm Infants

Christina J. Valentine, Georgia Morrow, Soledad Fernandez, Parul Gulati, Dennis Bartholomew, Don Long, Stephen E. Welty, Ardythe L. Morrow, Lynette K. Rogers

Journal:

The Journal of Pediatrics

Year:

2010

Language:

english

File:

PDF, 234 KB

english, 2010

2

Controlled induction of distributed microdeformation in wounded tissue via a microchamber array dressing

Bartholomew J. Kane, George Younan, Douglas Helm, Pouya Dastouri, Harrison Prentice-Mott, Daniel Irimia, Rodney K. Chan, Mehmet Toner, Dennis P. Orgill

Journal:

Journal of Biomedical Materials Research Part A

Year:

2010

Language:

english

File:

PDF, 2.35 MB

english, 2010

3

Unexpected detection of dystrophin gene deletions by array comparative genomic hybridization

Catherine E. Cottrell, Thomas W. Prior, Robert Pyatt, Caroline Astbury, Shalini Reshmi, Dennis Bartholomew, Joan Atkin, Kandamurugu Manickam, Devon Lamb Thrush, Matthew Pastore, Jerry Mendell, Chang-Y

Journal:

American Journal of Medical Genetics Part A

Year:

2010

Language:

english

File:

PDF, 264 KB

english, 2010

4

Design, Synthesis, and Catalytic Properties of Silica-Supported, Pt-Promoted Iron Fischer–Tropsch Catalysts

Jian Xu, Calvin H. Bartholomew, Jeremy Sudweeks, Dennis L. Eggett

Journal:

Topics in Catalysis

Year:

2003

Language:

english

File:

PDF, 497 KB

english, 2003

5

Mutations in PURA Cause Profound Neonatal Hypotonia, Seizures, and Encephalopathy in 5q31.3 Microdeletion Syndrome

Lalani, Seema R., Zhang, Jing, Schaaf, Christian P., Brown, Chester W., Magoulas, Pilar, Tsai, Anne Chun-Hui, El-Gharbawy, Areeg, Wierenga, Klaas J., Bartholomew, Dennis, Fong, Chin-To, Barbaro-Dieber

Journal:

The American Journal of Human Genetics

Year:

2014

Language:

english

File:

PDF, 389 KB

english, 2014

6

De novo mutations inbeta-catenin (CTNNB1)appear to be a frequent cause of intellectual disability: expanding the mutational and clinical spectrum

Kuechler, Alma, Willemsen, Marjolein H., Albrecht, Beate, Bacino, Carlos A., Bartholomew, Dennis W., van Bokhoven, Hans, van den Boogaard, Marie Jose H., Bramswig, Nuria, Büttner, Christian, Cremer, K

Journal:

Year:

2015

Language:

english

File:

PDF, 698 KB

english, 2015

7

A Randomized, Open-Label Pilot Study Comparing Desirudin and Argatroban in Patients With Suspected Heparin-Induced Thrombocytopenia With or Without Thrombosis: PREVENT-HIT Study

Boyce, Steven W, Bandyk, Dennis F, Bartholomew, John R, Frame, James N, Rice, Lawrence

Journal:

American Journal of Therapeutics

Year:

2011

Language:

english

File:

PDF, 266 KB

english, 2011

8

A de novo nonsense mutation in ASXL3 shared by siblings with Bainbridge-Ropers syndrome

Koboldt, Daniel C, Mihalic Mosher, Theresa, Kelly, Benjamin J, Sites, Emily, Bartholomew, Dennis, Hickey, Scott E, McBride, Kim, Wilson, Richard K, White, Peter

Journal:

Molecular Case Studies

Year:

2018

Language:

english

File:

PDF, 3.65 MB

english, 2018

9

Sample introduction in gas chromatography using a coiled wire filament

Tai V. Truong, Aaron N. Nackos, Jacolin A. Murray, Jon A. Kimball, Jason E. Hawkes, Donald J. Harvey, H. Dennis Tolley, Richard A. Robison, Calvin H. Bartholomew, Milton L. Lee

Journal:

Journal of Chromatography A

Year:

2009

Language:

english

File:

PDF, 562 KB

english, 2009

10

TCR Peptide Therapy in Human Autoimmune Diseases

Arthur A. Vandenbark, Elizabeth Morgan, Richard Bartholomew, Dennis Bourdette, Ruth Whitham, Dennis Carlo, Daniel Gold, George Hashim, Halina Offner

Journal:

Neurochemical Research

Year:

2001

Language:

english

File:

PDF, 77 KB

english, 2001

11

Identification of a Recurrent Microdeletion at 17q23.1q23.2 Flanked by Segmental Duplications Associated with Heart Defects and Limb Abnormalities

Blake C. Ballif, Aaron Theisen, Jill A. Rosenfeld, Ryan N. Traylor, Julie Gastier-Foster, Devon Lamb Thrush, Caroline Astbury, Dennis Bartholomew, Kim L. McBride, Robert E. Pyatt, Kate Shane, Wendy E.

Journal:

The American Journal of Human Genetics

Year:

2010

Language:

english

File:

PDF, 726 KB

english, 2010

12

Characterization of highly purified, inactivated HIV-1 particles isolated by anion exchange chromatography

Steven P. Richieri, Richard Bartholomew, Roland C. Aloia, Jay Savary, Richard Gore, John Holt, Francois Ferre, Roy Musil, H.R. Tian, Richard Trauger, Peter Lowry, Fred Jensen, Dennis J. Carlo, Robert

Journal:

Year:

1998

Language:

english

File:

PDF, 1.61 MB

english, 1998

13

Craniofacial-deafness-hand syndrome revisited

Annemarie Sommer, Dennis W. Bartholomew

Journal:

American Journal of Medical Genetics Part A

Year:

2003

Language:

english

File:

PDF, 258 KB

english, 2003

14

Matched unrelated donor transplantation in glycogen storage disease type 1b patient corrects severe neutropenia and recurrent infections

Mehyar, Lubna S., Abu-Arja, Rolla, Rangarajan, Hemalatha G., Pai, Vinita, Bartholomew, Dennis W., Rose, Melissa J., Bajwa, Rajinder P. S.

Journal:

Bone Marrow Transplantation

Year:

2018

Language:

english

File:

PDF, 439 KB

english, 2018

15

Infection Due to Paecilomyces lilacinus: A Challenging Clinical Identification

Camilla Saberhagen, Stephen A. Klotz, William Bartholomew, Dennis Drews and Anita Dixon

Journal:

Clinical Infectious Diseases

Year:

1997

Language:

english

File:

PDF, 275 KB

english, 1997

16

Iatrogenic Inner Ear Dehiscence After Lateral Skull Base Surgery

Bartholomew, Ryan A., Poe, Dennis, Dunn, Ian F., Smith, Timothy R., Corrales, Carleton Eduardo

Journal:

Otology & Neurotology

Year:

2019

File:

PDF, 457 KB

2019

17

Acute Dilated Cardiomyopathy in a Patient with Deficiency of Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase

Peter C. Dyke, Laura Konczal, Dennis Bartholomew, Kim L. McBride, Timothy M. Hoffman

Journal:

Pediatric Cardiology

Year:

2009

Language:

english

File:

PDF, 227 KB

english, 2009

18

Recurrent pancreatitis in ornithine transcarbamylase deficiency

Carlos E. Prada, Ajay Kaul, Robert J. Hopkin, Kimberley I. Page, Jaimie D. Nathan, Dennis W. Bartholomew, Mitchell B. Cohen, James E. Heubi, Nancy D. Leslie, T. Andrew Burrow

Journal:

Molecular Genetics and Metabolism

Year:

2012

Language:

english

File:

PDF, 128 KB

english, 2012

19

Cranial Nerve and Cervical Root Enhancement in an Infant With Polymerase Gamma Mutation Mitochondrial Disease

Horst, Deanna M., Ruess, Lynne, Rusin, Jerome A., Bartholomew, Dennis W.

Journal:

Pediatric Neurology

Year:

2014

Language:

english

File:

PDF, 668 KB

english, 2014

20

Characterization of the renal phenotype in RMND1 ‐related mitochondrial disease

Shayota, Brian J., Le, Nhon T., Bekheirnia, Nasim, Rosenfeld, Jill A., Goldstein, Amy C., Moritz, Michael, Bartholomew, Dennis W., Pastore, Matthew T., Xia, Fan, Eng, Christine, Yang, Yaping, Lamb, Do

Journal:

Molecular Genetics & Genomic Medicine

Year:

2019

File:

PDF, 565 KB

2019

21

Novel missense mutation in the coagulation factor IX catalytic domain associated with moderate disease

Dennis Bartholomew, Thomas Abshire, Melissa Fries, Alice Smith

Journal:

Year:

1997

Language:

english

File:

PDF, 75 KB

english, 1997

22

Cri du chat syndrome and complex karyotype in a patient with infantile spasms, hypsarrhythmia, nonketotic hyperglycinemia, and heterotopia

Chang Y. Tsao, Gail D. Wenger, Dennis W. Bartholomew

Journal:

American Journal of Medical Genetics Part A

Year:

2005

Language:

english

File:

PDF, 99 KB

english, 2005

23

Phenotypic spectrum of Costello syndrome individuals harboring the rare HRAS mutation p.Gly13Asp

Bertola, Débora, Buscarilli, Michelle, Stabley, Deborah L., Baker, Laura, Doyle, Daniel, Bartholomew, Dennis W., Sol-Church, Katia, Gripp, Karen W.

Journal:

American Journal of Medical Genetics Part A

Year:

2017

Language:

english

File:

PDF, 726 KB

english, 2017

24

Decreased FOXP3 levels in multiple sclerosis patients

Jianya Huan, Nicole Culbertson, Leslie Spencer, Richard Bartholomew, Gregory G. Burrows, Yuan K. Chou, Dennis Bourdette, Steven F. Ziegler, Halina Offner, Arthur A. Vandenbark

Journal:

Journal of Neuroscience Research

Year:

2005

Language:

english

File:

PDF, 330 KB

english, 2005

25

SRD5A3-CDG: Expanding the phenotype of a congenital disorder of glycosylation with emphasis on adult onset features

Wheeler, Patricia G., Ng, Bobby G., Sanford, Laura, Sutton, V. Reid, Bartholomew, Dennis W., Pastore, Matthew T., Bamshad, Michael J., Kircher, Martin, Buckingham, Kati J., Nickerson, Deborah A., Shen

Journal:

American Journal of Medical Genetics Part A

Year:

2016

Language:

english

File:

PDF, 597 KB

english, 2016

26

Changes in proteoglycan biosynthesis following leukocyte elastase treatment of bovine articular cartilage in culture

Dr. Jennifer S. Bartholomew, Dennis A. Lowther, Christopher J. Handley

Journal:

Arthritis & Rheumatism

Year:

1984

Language:

english

File:

PDF, 715 KB

english, 1984

27

Therapeutic approaches to cobalamin-C methylmalonic acidemia and homocystinuria

Dennis W. Bartholomew, Mark L. Batshaw, Robert H. Allen, Charles R. Roe, David Rosenblatt, David L. Valle, Clair A. Francomano

Journal:

The Journal of Pediatrics

Year:

1988

Language:

english

File:

PDF, 598 KB

english, 1988

28

Clinical course of sly syndrome (mucopolysaccharidosis type VII)

Montaño, Adriana M, Lock-Hock, Ngu, Steiner, Robert D, Graham, Brett H, Szlago, Marina, Greenstein, Robert, Pineda, Mercedes, Gonzalez-Meneses, Antonio, Çoker, Mahmut, Bartholomew, Dennis, Sands, Mark

Journal:

Journal of Medical Genetics

Year:

2016

Language:

english

File:

PDF, 7.00 MB

english, 2016

29

Vaccination with a CDR2 BV6S2/6S5 peptide in adjuvant induces peptide-specific T-cell responses in patients with multiple sclerosis

Elizabeth E. Morgan, Christopher J. Nardo, Jocelyn P. Diveley, Joel Kunin, Richard M. Bartholomew, Ronald B. Moss, Dennis J. Carlo

Journal:

Journal of Neuroscience Research

Year:

2001

Language:

english

File:

PDF, 87 KB

english, 2001

30

Therapeutic Vaccination with a Trivalent T Cell Receptor Peptide Vaccine Induces Peptide-specific IL-10-secreting T Cells, Restores Deficient Foxp3 Expression, and Induces Bystander Immunomodulation in Multiple Sclerosis Subjects

Arthur Vandenbark, Richard Bartholomew, Halina Offner, Dennis Bourdette

Journal:

Clinical Immunology

Year:

2007

Language:

english

File:

PDF, 40 KB

english, 2007

31

Prospective treatment of urea cycle disorders

Nancy E. Maestri, Elizabeth R. Hauser, Dennis Bartholomew, Saul W. Brusilow

Journal:

The Journal of Pediatrics

Year:

1991

Language:

english

File:

PDF, 621 KB

english, 1991

32

Allergens in School Settings: Results of Environmental Assessments in 3 City School Systems

Stuart L. Abramson, Anne Turner-Henson, Lise Anderson, Mary P. Hemstreet, L. Kay Bartholomew, Christine L. M. Joseph, Shenghui Tang, Shellie Tyrrell, Noreen M. Clark, Dennis Ownby

Journal:

Journal of School Health

Year:

2006

Language:

english

File:

PDF, 175 KB

english, 2006

33

Infection Due to Paecilomyces lilacinus : A Challenging Clinical Identification

Saberhagen, Camilla, Klotz, Stephen A., Bartholomew, William, Drews, Dennis, Dixon, Anita

Journal:

Clinical Infectious Diseases

Year:

1997

Language:

english

File:

PDF, 233 KB

english, 1997

34

RADIOIMMUNODETECTION STUDIES OF PROSTATE, COLON AND T-CELL LYMPHOMA TUMORS USING In-111 LABELED MONOCLONAL ANTITUMOR ANTIBODIES (In-111-MoAb); PRELIMINARY STUDIES

Halpern, Samuel E., Dillman, Robert O., Witztum, Kathryn F., Hagan, Phillip L., Dillman, Jacquelyn B., Clutter, Maureen L., Frincke, James M., Bartholomew, Richard M., David, Gary S., Carlo, Dennis J.

Journal:

Clinical Nuclear Medicine

Year:

1984

File:

PDF, 108 KB

1984

35

MCPH1 deletion in a newborn with severe microcephaly and premature chromosome condensation

Pfau, Ruthann B., Thrush, Devon Lamb, Hamelberg, Elizabeth, Bartholomew, Dennis, Botes, Shaun, Pastore, Matthew, Tan, Christopher, del Gaudio, Daniela, Gastier-Foster, Julie M., Astbury, Caroline

Journal:

European Journal of Medical Genetics

Year:

2013

Language:

english

File:

PDF, 756 KB

english, 2013

36

Severe cystic fibrosis associated with a AF508/R347H + D979A compound heterozygous genotype

Satoko Hojo, Jiro Fujita, Hiroshi Miyawaki, Yuka Obayashi, Jiro Takahara, Dennis W. Bartholomew

Journal:

Clinical Genetics

Year:

1998

Language:

english

File:

PDF, 332 KB

english, 1998

37

Fatigue damage analysis of notched carbon/epoxy composite by spate and finite element method

Pfau, Ruthann B., Thrush, Devon Lamb, Hamelberg, Elizabeth, Bartholomew, Dennis, Botes, Shaun, Pastore, Matthew, Tan, Christopher, del Gaudio, Daniela, Gastier-Foster, Julie M., Astbury, Caroline

Journal:

NDT & E International

Year:

1993

Language:

english

File:

PDF, 159 KB

english, 1993

38

Analysis of indications for referral to a multidisciplinary medical genetics clinic: Implications for training programs in obstetrics and gynecology

Bombard, Allan T., Rigdon, David T., Bartholomew, Dennis W., Flanagan, Judith C.

Journal:

American Journal of Obstetrics and Gynecology

Year:

1990

Language:

english

File:

PDF, 503 KB

english, 1990

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