S.E. Olpin: search on Z-Library

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1

Metabolic disorders presenting as liver disease

Simon Edward Olpin

Journal:

Paediatrics and Child Health

Year:

2010

Language:

english

File:

PDF, 105 KB

english, 2010

2

Gestational Trophoblastic Disease: Clinical and Imaging Features

Shaaban, Akram M., Rezvani, Maryam, Haroun, Reham R., Kennedy, Anne M., Elsayes, Khaled M., Olpin, Jeffrey D., Salama, Mohamed E., Foster, Bryan R., Menias, Christine O.

Journal:

Year:

2017

Language:

english

File:

PDF, 5.11 MB

english, 2017

3

Heterotopic Pancreas: Histopathologic Features, Imaging Findings, and Complications

Rezvani, Maryam, Menias, Christine, Sandrasegaran, Kumaresan, Olpin, Jeffrey D., Elsayes, Khaled M., Shaaban, Akram M.

Journal:

Year:

2017

Language:

english

File:

PDF, 3.07 MB

english, 2017

4

Imaging of Acute Pelvic Pain

Olpin, Jeffrey Dee, Strachowski, Loretta

Journal:

Radiologic Clinics of North America

Year:

2020

Language:

english

File:

PDF, 5.41 MB

english, 2020

5

Prenatal diagnosis of glutathione synthase deficiency

N. J. Manning, Mr N. P. Davies, S. E. Olpin, K. H. Carpenter, M. F. Smith, R. J. Pollitt, S. L. B. Duncan, A. Larsson, B. Carlsson

Journal:

Prenatal Diagnosis

Year:

1994

Language:

english

File:

PDF, 335 KB

english, 1994

6

Clinical, enzymatic and molecular characterization of nine new patients with malonyl-coenzyme A decarboxylase deficiency

G. S. Salomons, C. Jakobs, L. Landegge Pope, A. Errami, M. Potter, M. Nowaczyk, S. Olpin, N. Manning, J. A. J. Raiman, T. Slade, M. P. Champion, D. Peck, D. Gavrilov, R. Hillman, G. E. Hoganson, K. Do

Journal:

Journal of Inherited Metabolic Disease

Year:

2007

Language:

english

File:

PDF, 327 KB

english, 2007

7

Peroxisomal disorders

Camilla Scott, Simon Olpin

Journal:

Paediatrics and Child Health

Year:

2011

Language:

english

File:

PDF, 146 KB

english, 2011

8

The Distribution in Direction of Photoelectrons from Alkali Metal Surfaces

Ives, Herbert E., Olpin, A. R., Johnsrud, A. L.

Journal:

Physical Review (Series I)

Year:

1928

Language:

english

File:

PDF, 3.42 MB

english, 1928

9

Peroxisomal disorders

Scott, Camilla, Olpin, Simon

Journal:

Paediatrics and Child Health

Year:

2015

Language:

english

File:

PDF, 90 KB

english, 2015

10

Training of Physicists for Industrial Positions

Journal:

American Journal of Physics

Year:

1937

Language:

english

File:

PDF, 1.31 MB

english, 1937

11

Examining the Effectiveness of Psychological Strategies on Physiologic Markers: Evidence-Based Suggestions for Holistic Care of the Athlete

Dawson, Michelle A., Hamson-Utley, Jennifer Jordan, Hansen, Rodney, Olpin, Michael

Journal:

Journal of Athletic Training

Year:

2014

Language:

english

File:

PDF, 152 KB

english, 2014

12

Short-Chain Acyl-CoA Dehydrogenase Deficiency Associated with Early Onset Severe Axonal Neuropathy

Kurian, M. A., Hartley, L., Zolkipli, Z., Little, M. A., Costigan, D., Naughten, E. R., Olpin, S., Muntoni, F., King, M. D.

Journal:

Neuropediatrics

Year:

2004

Language:

english

File:

PDF, 65 KB

english, 2004

13

Beyond the Bowel: Extraintestinal Manifestations of Inflammatory Bowel Disease

Olpin, Jeffrey D., Sjoberg, Brett P., Stilwill, Sarah E., Jensen, Leif E., Rezvani, Maryam, Shaaban, Akram M.

Journal:

Year:

2017

Language:

english

File:

PDF, 4.57 MB

english, 2017

14

MR Imaging of Müllerian Fusion Anomalies

Olpin, Jeffrey D., Moeni, Aida, Willmore, Roderick J., Heilbrun, Marta E.

Journal:

Magnetic Resonance Imaging Clinics of North America

Year:

2017

Language:

english

File:

PDF, 1.89 MB

english, 2017

15

Nongynecologic Findings Seen at Pelvic US

Shaaban, Akram M., Rezvani, Maryam, Olpin, Jeffrey D., Kennedy, Anne M., Gaballah, Ayman H., Foster, Bryan R., Menias, Christine O., Elsayes, Khaled M.

Journal:

Year:

2017

Language:

english

File:

PDF, 6.23 MB

english, 2017

16

A comparison of 4 stress reduction modalities on measures of stress among university students

Bennion, Erica, Olpin, Michael N, DeBeliso, Mark, Coffey, Margaret, Roemer, EnidChung

Journal:

International Journal of Workplace Health Management

Year:

2018

Language:

english

File:

PDF, 453 KB

english, 2018

17

Child Meets Child: Social Interaction between School-Age Boys

Olpin, Michael, Kogan, Kate L.

Journal:

Perceptual and Motor Skills

Year:

1969

Language:

english

File:

PDF, 176 KB

english, 1969

18

Response to Finsterer: CPT-II deficiency needs to be detected in army personnel

Balasubramanian, M., Jenkins, T.M., Kirk, R.J., Nesbitt, I.M., Olpin, S.E., Hill, M., Gillett, G.T.

Journal:

Molecular Genetics and Metabolism Reports

Year:

2018

Language:

english

File:

PDF, 130 KB

english, 2018

19

Imaging and cancer of the cervix in low- and middle-income countries

Olpin, J., Chuang, L., Berek, J., Gaffney, D.

Journal:

Gynecologic Oncology Reports

Year:

2018

Language:

english

File:

PDF, 3.66 MB

english, 2018

20

Novel OCTN2 mutations: No genotype–phenotype correlations: Early carnitine therapy prevents cardiomyopathy

Anne-Marie Lamhonwah, Simon E. Olpin, Rodney J. Pollitt, Christine Vianey-Saban, Priscille Divry, Nathalie Guffon, Guy T. N. Besley, Russell Onizuka, Linda J. De Meirleir, Ljerka Cvitanovic-Sojat, Ivo

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 321 KB

english, 2002

21

Fumarase deficiency caused by homozygous P131R mutation and paternal partial isodisomy of chromosome 1

Wen-Qi Zeng, Hanlin Gao, Louise Brueton, Tim Hutchin, George Gray, Anupam Chakrapani, Simon Olpin, Vivian E. Shih

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 155 KB

english, 2006

22

Interstitial deletion of 1p22.2p31.1 and medium-chain acyl-CoA dehydrogenase deficiency in a patient with global developmental delay

Gustavo H.B. Maegawa, Nicola K. Poplawski, Brage Storstein Andresen, Simon E. Olpin, Gloria Nie, Joe T.R. Clarke, Ikuko Teshima

Journal:

American Journal of Medical Genetics Part A

Year:

2008

Language:

english

File:

PDF, 139 KB

english, 2008

23

Mitochondrial function and morphology are impaired in parkin-mutant fibroblasts

Heather Mortiboys, Kelly Jean Thomas, Werner J. H. Koopman, Stefanie Klaffke, Patrick Abou-Sleiman, Simon Olpin, Nicholas W. Wood, Peter H. G. M. Willems, Jan A. M. Smeitink, Mark R. Cookson, Oliver B

Journal:

Annals of Neurology

Year:

2008

Language:

english

File:

PDF, 517 KB

english, 2008

24

Analytical measurements of isopycnic density in the preparative ultacentrifuge with application to FeLV and FeLV-RNA

Jay L. Olpin, Charles L. Burger

Journal:

Analytical Biochemistry

Year:

1972

Language:

english

File:

PDF, 324 KB

english, 1972

25

Rapid stepwise solubilization and purification of type C retrovirus structural proteins by extraction with organic solvent

Jay L. Olpin, Stephen Oroszlan

Journal:

Analytical Biochemistry

Year:

1980

Language:

english

File:

PDF, 1.50 MB

english, 1980

26

Prenatal diagnosis of a defect in mediumchain fatty acid oxidation

R. J. Pollitt, N. J. Manning, S. E. Olpin, I. D. Young

Journal:

Journal of Inherited Metabolic Disease

Year:

1994

Language:

english

File:

PDF, 240 KB

english, 1994

27

A comparison of [9,10-3H]palmitic and [9,10-3H]myristic acids for the detection of defects of fatty acid oxidation in intact cultured fibroblasts

N. J. Manning, S. E. Olpin, R. J. Pollitt, J. Webley

Journal:

Journal of Inherited Metabolic Disease

Year:

1990

Language:

english

File:

PDF, 866 KB

english, 1990

28

Differential diagnosis of hydroxydicarboxylic aciduria based on release of3H2O from [9,10-3H]myristic and [9,10-3H]palmitic acids by intact cultured fibroblasts

S. E. Olpin, N. J. Manning, K. Carpenter, B. Middleton, R. J. Pollitt

Journal:

Journal of Inherited Metabolic Disease

Year:

1992

Language:

english

File:

PDF, 668 KB

english, 1992

29

Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency—diagnosis, plasma carnitine fractions and management in a further patient

R. Moore, J. F. T. Glasgow, M. A. Bingham, J. A. Dodge, R. J. Pollitt, S. E. Olpin, B. Middleton, K. Carpenter

Journal:

European Journal of Pediatrics

Year:

1993

Language:

english

File:

PDF, 454 KB

english, 1993

30

Hypertrophic pyloric stenosis: predicting the resolution of biochemical abnormalities

David J. Wilkinson, Richard A. Chapman, Anthony Owen, Simon Olpin, Sean S. Marven

Journal:

Pediatric Surgery International

Year:

2011

Language:

english

File:

PDF, 275 KB

english, 2011

31

Ornithine aminotransferase deficiency: Diagnostic difficulties in neonatal presentation

M. A. Cleary, L. Dorland, T. J. Koning, B. T. Poll-The, M. Duran, R. Mandell, V. E. Shih, R. Berger, S. E. Olpin, G. T. N. Besley

Journal:

Journal of Inherited Metabolic Disease

Year:

2005

Language:

english

File:

PDF, 115 KB

english, 2005

32

Biochemical, clinical and molecular findings in LCHAD and general mitochondrial trifunctional protein deficiency

S. E. Olpin, S. Clark, B. S. Andresen, C. Bischoff, R. K. J. Olsen, N. Gregersen, A. Chakrapani, M. Downing, N. J. Manning, M. Sharrard, J. R. Bonham, F. Muntoni, D. N. Turnbull, M. Pourfarzam

Journal:

Journal of Inherited Metabolic Disease

Year:

2005

Language:

english

File:

PDF, 132 KB

english, 2005

33

Hyperlipidaemia due to carnitine palmitoyltransferase I deficiency

H. Worthington, S. E. Olpin, I. Blumenthal, A. A. M. Morris

Journal:

Journal of Inherited Metabolic Disease

Year:

2007

Language:

english

File:

PDF, 109 KB

english, 2007

34

Carnitine transporter defect: Diagnosis in asymptomatic adult women following analysis of acylcarnitines in their newborn infants

S. Vijay, A. Patterson, S. Olpin, M. J. Henderson, S. Clark, C. Day, G. Savill, J. H. Walter

Journal:

Journal of Inherited Metabolic Disease

Year:

2006

Language:

english

File:

PDF, 191 KB

english, 2006

35

Cross-Sectional Imaging Obtained Immediately Following Radiofrequency Atrial Fibrillation Ablation Does Not Predict Endoscopic Evidence of Esophageal Injury

Darcie R. Gorman, Kathryn A. Peterson, John Fang, Jeffrey Olpin, Daniel O. Sommers, Molly McFadden, Jack H. Morshedzadeh, Nazem Akoum, Marcos Daccarett, Nassir Marrouche, Douglas G. Adler

Journal:

Digestive Diseases and Sciences

Year:

2011

Language:

english

File:

PDF, 247 KB

english, 2011

36

Fumarate hydratase mutations and predisposition to cutaneous leiomyomas, uterine leiomyomas and renal cancer

N.A. Alam, S. Olpin, I.M. Leigh

Journal:

British Journal of Dermatology

Year:

2005

Language:

english

File:

PDF, 90 KB

english, 2005

37

The Y42H mutation in medium-chain acyl-CoA dehydrogenase, which is prevalent in babies identified by MS/MS-based newborn screening, is temperature sensitive

Linda O'Reilly, Peter Bross, Thomas J. Corydon, Simon E. Olpin, Jakob Hansen, John M. Kenney, Shawn E. McCandless, Dianne M. Frazier, Vibeke Winter, Niels Gregersen, Paul C Engel, Brage Storstein Andr

Journal:

Year:

2004

Language:

english

File:

PDF, 656 KB

english, 2004

38

Carnitine-acylcarnitine translocase deficiency - a mild phenotype

S.E. Olpin, J.R. Bonham, M. Downing, N.J. Manning, R.J. Pollitt, M.J. Sharrard, M.S. Tanner

Journal:

Journal of Inherited Metabolic Disease

Year:

1997

Language:

english

File:

PDF, 6 KB

english, 1997

39

Improved detection of long-chain fatty acid oxidation defects in intact cells using [9,10-3H]oleic acid

S. E. Olpin, N. J. Manning, R. J. Pollitt, S. Clarke

Journal:

Journal of Inherited Metabolic Disease

Year:

1997

Language:

english

File:

PDF, 15 KB

english, 1997

40

Normal acylcarnitines in maternal urine during a pregnancy affected by glutaric aciduria type II

N. J. Manning, J. R. Bonham, M. Downing, R. G. Edwards, S. E. Olpin, R. J. Pollitt, M. Pourfarzam, M. J. Sharrard, M. S. Tanner

Journal:

Journal of Inherited Metabolic Disease

Year:

1999

Language:

english

File:

PDF, 35 KB

english, 1999

41

DNA-based prenatal diagnosis for very-long- chain acyl-CoA dehydrogenase deficiency

B. S. Andresen, S. Olpin, E. A. Kvittingen, P. Augoustides-Savvopoulou, D. Lindhout, D. J. J. Halley, C. Vianey-Saban, R. J. A. Wanders, L. IJlst, L. D. Schroeder, L. Bolund, N. Gregersen

Journal:

Journal of Inherited Metabolic Disease

Year:

1999

Language:

english

File:

PDF, 62 KB

english, 1999

42

Problems in the detection of fatty acid oxidation defects: Experience of a quality assurance programme for qualitative urinary organic acid analysis

M. Downing, J. C. Allen, J. R. Bonham, R. G. Edwards, N. J. Manning, S. E. Olpin, R. J. Pollitt

Journal:

Journal of Inherited Metabolic Disease

Year:

1999

Language:

english

File:

PDF, 51 KB

english, 1999

43

The diagnosis of carnitine palmitoyltransferase II deficiency is now possible in small skeletal muscle biopsies

I. P. Hargreaves, S. J. R. Heales, S. E. Olpin, J. A. Morgan-Hughes, J. M. Land

Journal:

Journal of Inherited Metabolic Disease

Year:

2000

Language:

english

File:

PDF, 48 KB

english, 2000

44

Fumarate hydratase deficiency: increased fumaric acid in amniotic fluid of two affected pregnancies

N. J. Manning, S. E. Olpin, R. J. Pollitt, M. Downing, A. F. Heeley, I. D. Young

Journal:

Journal of Inherited Metabolic Disease

Year:

2000

Language:

english

File:

PDF, 44 KB

english, 2000

45

Features of carnitine palmitoyltransferase type I deficiency

S. E. Olpin, J. Allen, J. R. Bonham, S. Clark, P. T. Clayton, J. Calvin, M. Downing, K. Ives, S. Jones, N. J. Manning, R. J. Pollitt, S. J. Standing, M. S. Tanner

Journal:

Journal of Inherited Metabolic Disease

Year:

2001

Language:

english

File:

PDF, 75 KB

english, 2001

46

2-Methyl-3-hydroxybutyryl-CoA dehydrogenase deficiency in a 23-year-old man

S. E. Olpin, R. J. Pollitt, J. Mcmenamin, N. J. Manning, G. Besley, J. P. N. Ruiter, R. J. A. Wanders

Journal:

Journal of Inherited Metabolic Disease

Year:

2002

Language:

english

File:

PDF, 73 KB

english, 2002

47

Renal tubular dysfunction in multiple acyl-CoA dehydrogenase deficiency

A. A. M. Morris, S. E. Olpin, W. G. Van't Hoff, A. W. Johnson, J. V. Leonard

Journal:

Journal of Inherited Metabolic Disease

Year:

1997

Language:

english

File:

PDF, 11 KB

english, 1997

48

MCAD deficiency in Denmark

Brage Storstein Andresen, Allan Meldgaard Lund, David Michael Hougaard, Ernst Christensen, Birthe Gahrn, Mette Christensen, Peter Bross, Anne Vested, Henrik Simonsen, Kristin Skogstrand, Simon Olpin,

Journal:

Molecular Genetics and Metabolism

Year:

2012

File:

PDF, 1.50 MB

2012

49

Lethal Cardiac Tachyarrhythmia in a Patient with Neonatal Carnitine–Acylcarnitine Translocase Deficiency

Choong, Karen, Clarke, J.T.R., Cutz, E., Pollit, R.J., Olpin, S.E.

Journal:

Pediatric and Developmental Pathology

Year:

2001

Language:

english

File:

PDF, 655 KB

english, 2001

50

Diagnostic difficulties in a case of primary systemic carnitine deficiency with idiopathic dilated cardiomyopathy

M Kinali, S.E Olpin, P.T Clayton, P.E.F Daubeney, E Mercuri, A.Y Manzur, I Tein, J Leonard, F Muntoni

Journal:

European Journal of Paediatric Neurology

Year:

2004

Language:

english

File:

PDF, 176 KB

english, 2004

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