Andrew T Hattersley: search on Z-Library

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

51

A successful transition to sulfonylurea treatment in male infant with neonatal diabetes caused by the novel abcc8 gene mutation and three years follow-up

Katanic, Dragan, Vorgučin, Ivana, Hattersley, Andrew, Ellard, Sian, Houghton, Jayne A.L., Obreht, Dragana, Knežević Pogančev, Marija, Vlaški, Jovan, Pavkov, Danijela

Journal:

Diabetes Research and Clinical Practice

Year:

2017

Language:

english

File:

PDF, 344 KB

english, 2017

52

KCNJ11 MUTATIONS CAUSE SEVERE NEUROPSYCHOLOGICAL DEFICITS

Day, Jacob, Torrens, Lorna, Bowman, Pamela, Shepherd, Maggie, Chakera, Ali, Hattersley, Andrew, Zeman, Adam

Journal:

Journal of Neurology Neurosurgery & Psychiatry

Year:

2016

Language:

english

File:

PDF, 53 KB

english, 2016

53

Genetic risk scores in adult-onset type 1 diabetes – Authors' reply

Thomas, Nicholas J, Jones, Samuel E, Weedon, Michael N, Shields, Beverley M, Hattersley, Andrew T, Oram, Richard A

Journal:

The Lancet Diabetes & Endocrinology

Year:

2018

Language:

english

File:

PDF, 334 KB

english, 2018

54

Excess mortality and cardiovascular disease in young adults with type 1 diabetes in relation to age at onset: a nationwide, register-based cohort study

Rawshani, Araz, Sattar, Naveed, Franzén, Stefan, Rawshani, Aidin, Hattersley, Andrew T, Svensson, Ann-Marie, Eliasson, Björn, Gudbjörnsdottir, Soffia

Journal:

Lancet (London, England)

Year:

2018

Language:

english

File:

PDF, 561 KB

english, 2018

55

A mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetes

de Wet, Heidi, Proks, Peter, Lafond, Mathilde, Aittoniemi, Jussi, Sansom, Mark S P, Flanagan, Sarah E, Pearson, Ewan R, Hattersley, Andrew T, Ashcroft, Frances M

Journal:

Year:

2008

Language:

english

File:

PDF, 349 KB

english, 2008

56

Type 2 Diabetes, SGLT2 Inhibitors, and Glucose Secretion

Phimister, Elizabeth G., Hattersley, Andrew T., Thorens, Bernard

Journal:

New England Journal of Medicine

Year:

2015

Language:

english

File:

PDF, 990 KB

english, 2015

57

Hypoplastic Glomerulocystic Kidney Disease and Hepatoblastoma

Abdul-Rahman, Omar A., Edghill, Emma L., Kwan, Andrea, Enns, Gregory M., Hattersley, Andrew T.

Journal:

Journal of Pediatric Hematology/Oncology

Year:

2009

Language:

english

File:

PDF, 76 KB

english, 2009

58

Macrosomia and Hyperinsulinaemic Hypoglycaemia in Patients with Heterozygous Mutations in the HNF4A Gene

Pearson, Ewan R, Boj, Sylvia F, Steele, Anna M, Barrett, Timothy, Stals, Karen, Shield, Julian P, Ellard, Sian, Ferrer, Jorge, Hattersley, Andrew T, Groop, Leif C

Journal:

Year:

2007

Language:

english

File:

PDF, 260 KB

english, 2007

59

Permanent Neonatal Diabetes due to Paternal Germline Mosaicism for an Activating Mutation of the KCNJ11 Gene Encoding the Kir6.2 Subunit of the β-Cell Potassium Adenosine Triphosphate Channel

Gloyn, Anna L., Cummings, Elizabeth A., Edghill, Emma L., Harries, Lorna W., Scott, Rachel, Costa, Teresa, Temple, I. Karen, Hattersley, Andrew T., Ellard, Sian

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2004

Language:

english

File:

PDF, 110 KB

english, 2004

60

Common Variation in the DIO2 Gene Predicts Baseline Psychological Well-Being and Response to Combination Thyroxine Plus Triiodothyronine Therapy in Hypothyroid Patients

Panicker, Vijay, Saravanan, Ponnusamy, Vaidya, Bijay, Evans, Jonathan, Hattersley, Andrew T., Frayling, Timothy M., Dayan, Colin M.

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2009

Language:

english

File:

PDF, 111 KB

english, 2009

61

Maternal hypothyroxinaemia in pregnancy is associated with obesity and adverse maternal metabolic parameters

Knight, Bridget A, Shields, Beverley M, Hattersley, Andrew T, Vaidya, Bijay

Journal:

European Journal of Endocrinology

Year:

2016

Language:

english

File:

PDF, 108 KB

english, 2016

62

Crossover studies can help the individualisation of care in type 2 diabetes: the MASTERMIND approach

Angwin, Catherine, Pearson, Ewan, Hattersley, Andrew

Journal:

Practical Diabetes

Year:

2016

Language:

english

File:

PDF, 411 KB

english, 2016

63

Screening for neonatal diabetes at day 5 of life using dried blood spot glucose measurement

McDonald, Timothy J., Besser, Rachel E., Perry, Mandy, Babiker, Tarig, Knight, Bridget A., Shepherd, Maggie H., Ellard, Sian, Flanagan, Sarah E., Hattersley, Andrew T.

Journal:

Year:

2017

Language:

english

File:

PDF, 419 KB

english, 2017

64

Mutations in the VNTR of the carboxyl-ester lipase gene (CEL) are a rare cause of monogenic diabetes

Janniche Torsvik, Stefan Johansson, Anders Johansen, Jakob Ek, Jayne Minton, Helge Ræder, Sian Ellard, Andrew Hattersley, Oluf Pedersen, Torben Hansen, Anders Molven, Pål R. Njølstad

Journal:

Year:

2010

Language:

english

File:

PDF, 309 KB

english, 2010

65

Neonatal hyperinsulinaemic hypoglycaemia and monogenic diabetes due to a heterozygous mutation of the HNF4A gene

Jennifer J. CONN, Peter J. SIMM, Jeremy J. N. OATS, Alison J. NANKERVIS, Susan E. JACOBS, Sian ELLARD, Andrew T. HATTERSLEY

Journal:

Australian and New Zealand Journal of Obstetrics and Gynaecology

Year:

2009

Language:

english

File:

PDF, 976 KB

english, 2009

66

10.1038/74307

Turnpenny, Peter D., Bulman, Michael P., Kusumi, Kenro, Frayling, Timothy M., McKeown, Carole, Garrett, Christine, Lander, Eric S., Krumlauf, Robb, Hattersley, Andrew T., Ellard, Sian

Journal:

Nature Genetics

Year:

2000

Language:

english

File:

PDF, 883 KB

english, 2000

67

Mutations in PTF1A cause pancreatic and cerebellar agenesis

Sellick, Gabrielle S, Barker, Karen T, Stolte-Dijkstra, Irene, Fleischmann, Christina, J Coleman, Richard, Garrett, Christine, Gloyn, Anna L, Edghill, Emma L, Hattersley, Andrew T, Wellauer, Peter K

Journal:

Nature Genetics

Year:

2004

Language:

english

File:

PDF, 582 KB

english, 2004

68

A conserved tryptophan at the membrane–water interface acts as a gatekeeper for Kir6.2/SUR1 channels and causes neonatal diabetes when mutated

Roope Männikkö, Phillip J. Stansfeld, Alexandra S. Ashcroft, Andrew T. Hattersley, Mark S. P. Sansom, Sian Ellard, Frances M. Ashcroft

Journal:

The Journal of Physiology

Year:

2011

Language:

english

File:

PDF, 795 KB

english, 2011

69

Early-onset, severe lipoatrophy in a patient with permanent neonatal diabetes mellitus secondary to a recessive mutation in the INS gene

Marianna Rachmiel, Oscar Rubio-Cabezas, Sian Ellard, Andrew T Hattersley, Kusiel Perlman

Journal:

Pediatric Diabetes

Year:

2012

Language:

english

File:

PDF, 542 KB

english, 2012

70

Development of a bloodspot assay for insulin

Nicola L. Butter, Andrew T. Hattersley, Penelope M. Clark

Journal:

Clinica Chimica Acta

Year:

2001

Language:

english

File:

PDF, 145 KB

english, 2001

71

A Gene for Autosomal Recessive Spondylocostal Dysostosis Maps to 19q13.1-q13.3

Peter D. Turnpenny, Michael P. Bulman, Timothy M. Frayling, Tewfiq K. Abu-Nasra, Christine Garrett, Andrew T. Hattersley, Sian Ellard

Journal:

The American Journal of Human Genetics

Year:

1999

Language:

english

File:

PDF, 279 KB

english, 1999

72

Clinical implications of a molecular genetic classification of monogenic β-cell diabetes

Murphy, Rinki, Ellard, Sian, Hattersley, Andrew T

Journal:

Nature Clinical Practice Endocrinology and Metabolism

Year:

2008

Language:

english

File:

PDF, 440 KB

english, 2008

73

Permanent neonatal diabetes mellitus: prevalence and genetic diagnosis in the SEARCH for Diabetes in Youth Study

Shankar, Roopa Kanakatti, Pihoker, Catherine, Dolan, Lawrence M., Standiford, Debra, Badaru, Angela, Dabelea, Dana, Rodriguez, Beatriz, Black, Mary Helen, Imperatore, Giuseppina, Hattersley, Andrew, E

Journal:

Pediatric Diabetes

Year:

2012

Language:

english

File:

PDF, 520 KB

english, 2012

74

Origin of de Novo KCNJ11 Mutations and Risk of Neonatal Diabetes for Subsequent Siblings

Edghill, Emma L., Gloyn, Anna L., Goriely, Anne, Harries, Lorna W., Flanagan, Sarah E., Rankin, Julia, Hattersley, Andrew T., Ellard, Sian

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2007

Language:

english

File:

PDF, 188 KB

english, 2007

75

Reevaluation of a case of type 1 diabetes mellitus diagnosed before 6 months of age

Jones, Angus G., Hattersley, Andrew T.

Journal:

Nature Reviews Endocrinology (formerly Nature Clinical Practice Endocrinology & Metabolism)

Year:

2010

Language:

english

File:

PDF, 193 KB

english, 2010

76

Population-Based Assessment of a Biomarker-Based Screening Pathway to Aid Diagnosis of Monogenic Diabetes in Young-Onset Patients

Shields, Beverley M., Shepherd, Maggie, Hudson, Michelle, McDonald, Timothy J., Colclough, Kevin, Peters, Jaime, Knight, Bridget, Hyde, Chris, Ellard, Sian, Pearson, Ewan R., Hattersley, Andrew T.

Journal:

Year:

2017

Language:

english

File:

PDF, 1.13 MB

english, 2017

77

C-Peptide Decline in Type 1 Diabetes Has Two Phases: An Initial Exponential Fall and a Subsequent Stable Phase

Shields, Beverley M., McDonald, Timothy J., Oram, Richard, Hill, Anita, Hudson, Michelle, Leete, Pia, Pearson, Ewan R., Richardson, Sarah J., Morgan, Noel G., Hattersley, Andrew T.

Journal:

Year:

2018

Language:

english

File:

PDF, 856 KB

english, 2018

78

PLIN1 Haploinsufficiency Is Not Associated With Lipodystrophy

Laver, Thomas W, Patel, Kashyap A, Colclough, Kevin, Curran, Jacqueline, Dale, Jane, Davis, Nikki, Savage, David B, Flanagan, Sarah E, Ellard, Sian, Hattersley, Andrew T, Weedon, Michael N

Journal:

Journal of Clinical Endocrinology & Metabolism

Year:

2018

Language:

english

File:

PDF, 348 KB

english, 2018

79

Proposed mechanism for a novel insertion/deletion frameshift mutation (I414G415ATCG→CCA) in the hepatocyte nuclear factor 1 alpha (HNF-1α) gene which causes maturity-onset diabetes of the young (MODY)

Sian Ellard, Michael P. Bulman, Timothy M. Frayling, Maggie Shepherd, Andrew T. Hattersley

Journal:

Year:

2000

Language:

english

File:

PDF, 130 KB

english, 2000

80

Boride cluster fusion through copper and silver. Crystal structure of [(Ph3P)2N][(HRu4(CO)12BH)2Ag]

Catherine E Housecroft, Sylvia M Draper, Andrew D Hattersley, Arnold L Rheingold

Journal:

Journal of Organometallic Chemistry

Year:

2000

Language:

english

File:

PDF, 152 KB

english, 2000

81

Tall stories: the fundamental difficulties of genetic association studies

Michael N. Weedon, Andrew T. Hattersley, Timothy M. Frayling

Journal:

Clinical Endocrinology

Year:

2004

Language:

english

File:

PDF, 168 KB

english, 2004

82

Persistently autoantibody negative (PAN) type 1 diabetes mellitus in children

Shihab Hameed, Sian Ellard, Helen J Woodhead, Kristen A Neville, Jan L Walker, Maria E Craig, Taylor Armstrong, Liping Yu, George S Eisenbarth, Andrew T Hattersley, Charles F Verge

Journal:

Pediatric Diabetes

Year:

2011

Language:

english

File:

PDF, 519 KB

english, 2011

83

10.1038/74321

Turnpenny, Peter D., Bulman, Michael P., Kusumi, Kenro, Frayling, Timothy M., McKeown, Carole, Garrett, Christine, Lander, Eric S., Krumlauf, Robb, Hattersley, Andrew T., Ellard, Sian

Journal:

Nature Biotechnology

Year:

2000

Language:

english

File:

PDF, 95 KB

english, 2000

84

Functional analysis of mutations in PDX1 found in patients with type II diabetes

Susan C Campbell, Louisa Shepherd, Leif Groop, Andrew T Hattersley, Wendy M Macfarlane

Journal:

Diabetes Research and Clinical Practice

Year:

2000

Language:

english

File:

PDF, 278 KB

english, 2000

85

Evidence for Linkage of Stature to Chromosome 3p26 in a Large U.K. Family Data Set Ascertained for Type 2 Diabetes

Steven Wiltshire, Timothy M. Frayling, Andrew T. Hattersley, Graham A. Hitman, Mark Walker, Jonathan C. Levy, Stephen O'Rahilly, Christopher J. Groves, Stephan Menzel, Lon R. Cardon, Mark I. McCarthy

Journal:

The American Journal of Human Genetics

Year:

2002

Language:

english

File:

PDF, 165 KB

english, 2002

86

Permanent neonatal diabetes misdiagnosed as type 1 diabetes in a 28-year-old female: A life-changing diagnosis

Thewjitcharoen, Yotsapon, Wanothayaroj, Ekgaluck, Himathongkam, Thep, Flanagan, Sarah E., Ellard, Sian, Hattersley, Andrew T.

Journal:

Diabetes Research and Clinical Practice

Year:

2014

Language:

english

File:

PDF, 186 KB

english, 2014

87

Chromosome 17q12 microdeletions but not intragenic HNF1B mutations link developmental kidney disease and psychiatric disorder

Clissold, Rhian L., Shaw-Smith, Charles, Turnpenny, Peter, Bunce, Benjamin, Bockenhauer, Detlef, Kerecuk, Larissa, Waller, Simon, Bowman, Pamela, Ford, Tamsin, Ellard, Sian, Hattersley, Andrew T., Bin

Journal:

Kidney International

Year:

2016

Language:

english

File:

PDF, 935 KB

english, 2016

88

A UK nationwide prospective study of treatment change in MODY: genetic subtype and clinical characteristics predict optimal glycaemic control after discontinuing insulin and metformin

Shepherd, Maggie H., Shields, Beverley M., Hudson, Michelle, Pearson, Ewan R., Hyde, Christopher, Ellard, Sian, Hattersley, Andrew T., Patel, Kashyap A.

Journal:

Year:

2018

Language:

english

File:

PDF, 896 KB

english, 2018

89

Variants in the aromatase gene and on the Y-chromosome are not associated with adult height or insulin resistance in a UK population

Michael N. Weedon, Martina Turner, Beatrice Knight, Penny Clark, Andrew T. Hattersley, Timothy M. Frayling

Journal:

Clinical Endocrinology

Year:

2003

Language:

english

File:

PDF, 83 KB

english, 2003

90

FTOgene variation and measures of body mass in an African population

Branwen J Hennig, Anthony J Fulford, Giorgio Sirugo, Pura Rayco-Solon, Andrew T Hattersley, Timothy M Frayling, Andrew M Prentice

Journal:

BMC Medical Genetics

Year:

2009

Language:

english

File:

PDF, 553 KB

english, 2009

91

The HOPE study and diabetes

Gerry Fegan, David Ward, Leo Clarke, Kenneth MacLeod, Andrew Hattersley

Journal:

Year:

2000

Language:

english

File:

PDF, 60 KB

english, 2000

92

Pigmentary retinal dystrophy and the syndrome of maternally inherited diabetes and deafness caused by the mitochondrial DNA 3243 tRNALeu A to G mutation

Paul R Smith, Stephen C Bain, Peter A Good, Andrew T Hattersley, Anthony H Barnett, Jon M Gibson, Paul M Dodson

Journal:

Year:

1999

Language:

english

File:

PDF, 450 KB

english, 1999

93

The role of the HNF4α enhancer in type 2 diabetes: variants of the HNF4α enhancer are not a common cause of susceptibility to type 2 diabetes

Simon M.S Mitchell, Anna L Gloyn, Katharine R Owen, Andrew T Hattersley, Timothy M Frayling

Journal:

Molecular Genetics and Metabolism

Year:

2002

Language:

english

File:

PDF, 73 KB

english, 2002

94

Cardiovascular prevention in type 2 diabetes mellitus, Are we succeeding?

Fegan, Gerry, Ward, David, Clarke, Leo, MacLeod, Kenneth, Hattersley, Andrew

Journal:

Diabetes Research and Clinical Practice

Year:

2000

Language:

english

File:

PDF, 103 KB

english, 2000

95

Fetal Macrosomia and Neonatal Hyperinsulinemic Hypoglycemia Associated With Transplacental Transfer of Sulfonylurea in a Mother With KCNJ11 -Related Neonatal Diabetes

Myngheer, Nele, Allegaert, Karel, Hattersley, Andrew, McDonald, Tim, Kramer, Holger, Ashcroft, Frances M., Verhaeghe, Johan, Mathieu, Chantal, Casteels, Kristina

Journal:

Year:

2014

Language:

english

File:

PDF, 567 KB

english, 2014

96

Boride cluster fusion via an M4-unit (M = Cu or Ag): molecular structure of [ppn][{Ru4H(CO)12B}2Cu4(�-Cl)][Cl][ppn =(PPh3)2N]

Draper, Sylvia M., Hattersley, Andrew D., Housecroft, Catherine E., Rheingold, Arnold L.

Journal:

Journal of the Chemical Society Chemical Communications

Year:

1992

Language:

english

File:

PDF, 374 KB

english, 1992

97

The value of in vitro studies in a case of neonatal diabetes with a novel Kir6.2-W68G mutation

O'Connell, Susan M., Proks, Peter, Kramer, Holger, Mattis, Katia K., Sachse, Gregor, Joyce, Caroline, Houghton, Jayne A. L., Ellard, Sian, Hattersley, Andrew T., Ashcroft, Frances M., O'Riordan, Steph

Journal:

Clinical Case Reports

Year:

2015

Language:

english

File:

PDF, 359 KB

english, 2015

98

Biallelic RFX6 mutations can cause childhood as well as neonatal onset diabetes mellitus

Sansbury, Francis H, Kirel, Birgül, Caswell, Richard, Lango Allen, Hana, Flanagan, Sarah E, Hattersley, Andrew T, Ellard, Sian, Shaw-Smith, Charles J

Journal:

European Journal of Human Genetics

Year:

2015

Language:

english

File:

PDF, 66 KB

english, 2015

99

A Mendelian Randomization Study Provides Evidence that Adiposity and Dyslipidemia Lead to Lower Urinary Albumin Creatinine Ratio, a Marker of Microvascular Function

Casanova, Francesco, Wood, Andrew R., Yaghootkar, Hanieh, Beaumont, Robert N., Jones, Samuel E., Gooding, Kim M., Aizawa, Kunihiko, Strain, W. David, Hattersley, Andrew T., Khan, Faisel, Shore, Angela

Journal:

Year:

2020

File:

PDF, 1.08 MB

2020

100

Response to treatment with rosiglitazone in familial partial lipodystrophy due to a mutation in the LMNA gene

Katharine R. Owen, Mollie Donohoe, Sian Ellard, Andrew T. Hattersley

Journal:

Diabetic Medicine

Year:

2003

Language:

english

File:

PDF, 97 KB

english, 2003

To build up a library is to create a life. It’s never just a random collection of books.

— Carlos María Domínguez

Official channel

Z-Library Desktop Launcher

Z-Library Since 2009 support@1delivery.pm

EnglishРусскийEspañolItalianoελληνικάاللغة العربيةBahasa IndonesiaBahasa Malaysiaहिन्दीDeutschFrançaisPortuguêsУкраїнськаPolski中文繁體中文日本語Tiếng ViệtAzərbaycan DiliՀայոց լեզուภาษาไทยTürk Diliქართველიবাংলাپښتوతెలుగుاردو한국어SrpskiБългарски