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34 results for Barrett,+Timothy+G

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Books
Reinventing (with) theory in rhetoric and writing studies : essays in honor of Sharon Crowley / edited by Andrea Alden, Kendall Gerdes, Judy Holiday, Ryan Skinnell.
Publisher:Logan : Utah State University Press, [2019]
Call Numbers:G 2019/5669
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Books
Comprehensive women's mental health / edited by David J. Castle, Kathryn M. Abel.
Publisher:Cambridge, United Kingdom : Cambridge University Press, 2016.
Call Numbers:G 2016/2080
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Books
The Cambridge history of English poetry / edited by Michael O'Neill.
Publisher:Cambridge, U.K. ; New York, [N.Y.] : Cambridge University Press, 2010.
Date:2010.
Call Numbers:N821.009/76
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Books
Know this : today's most interesting and important scientific ideas, discoveries, and developments / edited by John Brockman.
Publisher:New York : Harper Perennial, [2017]
Edition:First edition.
Call Numbers:G 2017/1341
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Legacies and mega events : fact or fairy tales? / edited by Ian Brittain, Jason Bocarro, Terri Byers, and Kamilla Swart.
Publisher:Abingdon, Oxon ; New York, NY : Routledge, an imprint of the Taylor & Francis Group, 2018.
Call Numbers:G 2018/0329
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A history of English autobiography / edited by Adam Smyth, Oxford University.
Publisher:New York, NY, USA : Cambridge University Press, 2016.
Call Numbers:G 2016/2819
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ArticlesPeer ReviewedFull Text
Rising Incidence of Type 2 Diabetes in Children in the U.K
Author / Creator:Haines, Linda ; Wan, Kay Chong ; Lynn, Richard ; Barrett, Timothy G ; Shield, Julian P.H
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2007-05, Vol.30 (5), p.1097-1101
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Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation
Author / Creator:Friesema, Edith CH ; Grueters, Annette ; Biebermann, Heike ; Krude, Heiko ; von Moers, Arpad ; Reeser, Maarten ; Barrett, Timothy G ; Mancilla, Edna E ; Svensson, Johan ; Kester, Monique HA ; Kuiper, George GJM ; Balkassmi, Sahila ; Uitterlinden, André G ; Koehrle, Josef ; Rodien, Patrice ; Halestrap, Andrew P ; Visser, Theo J
Publisher:London: Elsevier Ltd
Journal title:The Lancet (British edition), 2004-10, Vol.364 (9443), p.1435-1437
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Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model
Author / Creator:Chen, Jian-Hua ; Goh, Kim Jee ; Rocha, Nuno ; Groeneveld, Matthijs P. ; Minic, Marina ; Barrett, Timothy G. ; Savage, David ; Semple, Robert K.
Publisher:England: The Company of Biologists Ltd
Journal title:Disease models & mechanisms, 2017-12, Vol.10 (12), p.1411-1420
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Prevalence of Abnormal Lipid Profiles and the Relationship With the Development of Microalbuminuria in Adolescents With Type 1 Diabetes
Author / Creator:Loredana Marcovecchio, M ; Neil Dalton, R ; Toby Prevost, A ; Acerini, Carlo L ; Barrett, Timothy G ; Cooper, Jason D ; Edge, Julie ; Neil, Andrew ; Shield, Julian ; Widmer, Barry ; Todd, John A ; Dunger, David B
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2009-04, Vol.32 (4), p.658-663
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EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome
Author / Creator:Farmer, Amy ; Aymé, Ségolène ; de Heredia, Miguel Lopez ; Maffei, Pietro ; McCafferty, Susan ; Młynarski, Wojciech ; Nunes, Virginia ; Parkinson, Kay ; Paquis-Flucklinger, Véronique ; Rohayem, Julia ; Sinnott, Richard ; Tillmann, Vallo ; Tranebjærg, Lisbeth ; Barrett, Timothy G
Publisher:England: BioMed Central
Journal title:BMC pediatrics, 2013-08, Vol.13 (1), p.130-130, Article 130
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Maternal but Not Paternal Association of Ambulatory Blood Pressure With Albumin Excretion in Young Offspring With Type 1 Diabetes
Author / Creator:Marcovecchio, M. Loredana ; Tossavainen, Paivi H ; Acerini, Carlo L ; Barrett, Timothy G ; Edge, Julie ; Neil, Andrew ; Shield, Julian ; Widmer, Barry ; Dalton, R. Neil ; Dunger, David B
Publisher:Alexandria, VA: American Diabetes Association
Journal title:Diabetes care, 2010-02, Vol.33 (2), p.366-371
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ArticlesPeer ReviewedFull Text
Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomes
Author / Creator:Skinner, Timothy C ; Lange, Karin S ; Hoey, Hilary ; Mortensen, Henrik B ; Aanstoot, Henk‐Jan ; Castaňo, Luis ; Skovlund, Soren ; Swift, Peter GF ; Cameron, Fergus J ; Dorchy, Harry R ; Palmert, Mark R ; Kaprio, Eero ; Robert, Jean‐Jacques ; Danne, Thomas ; Neu, Andreas ; Shalitin, Shlomit ; Chiarelli, Francesco ; Chiari, Giovanni ; Urakami, Tatsuhiko ; Njølstad, Pål R ; Jarosz‐Chobot, Premyslawa K ; Roche, Edna F ; Castro‐Correia, Cintia G ; Kocova, Mirjana ; Åman, Jan ; Schönle, Eugen ; Barrett, Timothy G ; Fisher, Lynda ; de Beaufort, Carine E
Journal title:Pediatric diabetes, 2018-05, Vol.19 (3), p.559-565
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Clinical utility gene card for: Alström Syndrome - update 2013
Author / Creator:Marshall, Jan D ; Maffei, Pietro ; Beck, Sebastian ; Barrett, Timothy G ; Paisey, Richard ; Naggert, Jürgen K
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2013-11, Vol.21 (11), p.3-4
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ArticlesPeer ReviewedFull Text
Treatment adherence and BMI reduction are key predictors of HbA1c 1 year after diagnosis of childhood type 2 diabetes in the United Kingdom
Author / Creator:Candler, Toby P. ; Mahmoud, Osama ; Lynn, Richard M. ; Majbar, Abdalmonen A. ; Barrett, Timothy G. ; Shield, Julian P. H.
Publisher:Former Munksgaard: John Wiley & Sons A/S
Journal title:Pediatric diabetes, 2018-12, Vol.19 (8), p.1393-1399
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ArticlesPeer ReviewedFull Text
Comparison of the clinical scoring systems in Silver–Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing
Author / Creator:Dias, Renuka P ; Nightingale, Peter ; Hardy, Carol ; Kirby, Gail ; Tee, Louise ; Price, Susan ; MacDonald, Fiona ; Barrett, Timothy G ; Maher, Eamonn R
Publisher:England: BMJ Publishing Group Ltd
Journal title:Journal of medical genetics, 2013-09, Vol.50 (9), p.635-639
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ArticlesPeer ReviewedFull Text
Refining genotype–phenotype correlation in Alström syndrome through study of primary human fibroblasts
Author / Creator:Chen, Jian‐Hua ; Geberhiwot, Tarekegn ; Barrett, Timothy G. ; Paisey, Richard ; Semple, Robert K.
Publisher:United States: John Wiley & Sons, Inc
Journal title:Molecular genetics & genomic medicine, 2017-07, Vol.5 (4), p.390-404
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ArticlesPeer ReviewedFull Text
Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486) causing severe Wolfram syndrome and first report of male fertility
Author / Creator:Haghighi, Amirreza ; Haghighi, Alireza ; Setoodeh, Aria ; Saleh-Gohari, Nasrollah ; Astuti, Dewi ; Barrett, Timothy G
Publisher:England: Nature Publishing Group
Journal title:European journal of human genetics : EJHG, 2013-03, Vol.21 (3), p.347-351
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A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects
Author / Creator:Cangul, Hakan ; Bas, Veysel N. ; Saglam, Yaman ; Kendall, Michaela ; Barrett, Timothy G. ; Maher, Eamonn R. ; Aycan, Zehra
Publisher:Germany: De Gruyter
Journal title:Journal of Pediatric Endocrinology & Metabolism, 2014-11, Vol.27 (11), p.1101-1105
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ArticlesPeer ReviewedFull Text
Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomes
Author / Creator:Skinner, Timothy C ; Lange, Karin S ; Hoey, Hilary ; Mortensen, Henrik B ; Aanstoot, Henk‐Jan ; Castaňo, Luis ; Skovlund, Soren ; Swift, Peter GF ; Cameron, Fergus J ; Dorchy, Harry R ; Palmert, Mark R ; Kaprio, Eero ; Robert, Jean‐Jacques ; Danne, Thomas ; Neu, Andreas ; Shalitin, Shlomit ; Chiarelli, Francesco ; Chiari, Giovanni ; Urakami, Tatsuhiko ; Njølstad, Pål R ; Jarosz‐Chobot, Premyslawa K ; Roche, Edna F ; Castro‐Correia, Cintia G ; Kocova, Mirjana ; Åman, Jan ; Schönle, Eugen ; Barrett, Timothy G ; Fisher, Lynda ; de Beaufort, Carine E
Publisher:Former Munksgaard: John Wiley & Sons A/S
Journal title:Pediatric diabetes, 2018-05, Vol.19 (3), p.559-565
View online as a Library member
Access ebook if you are in the Library. Registered NSW residents may log in from home.

Showing 1 to 20 of 34 results

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Reinventing (with) theory in rhetoric and writing studies : essays in honor of Sharon Crowley / edited by Andrea Alden, Kendall Gerdes, Judy Holiday, Ryan Skinnell.

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Comprehensive women's mental health / edited by David J. Castle, Kathryn M. Abel.

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The Cambridge history of English poetry / edited by Michael O'Neill.

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Know this : today's most interesting and important scientific ideas, discoveries, and developments / edited by John Brockman.

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Legacies and mega events : fact or fairy tales? / edited by Ian Brittain, Jason Bocarro, Terri Byers, and Kamilla Swart.

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A history of English autobiography / edited by Adam Smyth, Oxford University.

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Rising Incidence of Type 2 Diabetes in Children in the U.K

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Association between mutations in a thyroid hormone transporter and severe X-linked psychomotor retardation

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Evaluation of human dermal fibroblasts directly reprogrammed to adipocyte-like cells as a metabolic disease model

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Prevalence of Abnormal Lipid Profiles and the Relationship With the Development of Microalbuminuria in Adolescents With Type 1 Diabetes

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EURO-WABB: an EU rare diseases registry for Wolfram syndrome, Alström syndrome and Bardet-Biedl syndrome

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Maternal but Not Paternal Association of Ambulatory Blood Pressure With Albumin Excretion in Young Offspring With Type 1 Diabetes

Export this record

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Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomes

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Clinical utility gene card for: Alström Syndrome - update 2013

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Treatment adherence and BMI reduction are key predictors of HbA1c 1 year after diagnosis of childhood type 2 diabetes in the United Kingdom

Export this record

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Comparison of the clinical scoring systems in Silver–Russell syndrome and development of modified diagnostic criteria to guide molecular genetic testing

Export this record

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Refining genotype–phenotype correlation in Alström syndrome through study of primary human fibroblasts

Export this record

Export record to excel

Identification of homozygous WFS1 mutations (p.Asp211Asn, p.Gln486) causing severe Wolfram syndrome and first report of male fertility

Export this record

Export record to excel

A nonsense thyrotropin receptor gene mutation (R609X) is associated with congenital hypothyroidism and heart defects

Export this record

Export record to excel

Targets and teamwork: Understanding differences in pediatric diabetes centers treatment outcomes

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