Bibliografia UJ CM



Zapytanie: ELLARD S
Liczba odnalezionych rekordów: 7



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B.M. Shields, T. Mcdonald, K. Owen, M[aciej] Malecki, R. Besser, A. Jones, S. Ellard, W. Henley, A. Hattersley.
A clinical diagnostic model using biomarkers and clinical characteristics for the identification of MODY patients.
W: International Society for Clinical Biostatistics 35th Annual Conference, Vienna, Austria, 24-28 August 2014 : abstract book.
s. 126 : abstr. P3.5.145.
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A.S. Slingerland, B.M. Shields, S.E. Flanagan, G.J. Bruining, K. Noordam, A. Gach, W. Mlynarski, M[aciej] T. Malecki, A.T. Hattersley, S. Ellard.
Referral rates for diagnostic testing support an incidence of permanent neonatal diabetes in three European countries of at least 1 in 260,000 live births.
Diabetologia
2009 : Vol. 52, nr 8, s. 1683-1685, il., bibliogr. 9 poz.
p-ISSN: 0012-186X
LR
AIF
IF: 6.551
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S. Ellard, C. Bellanne-Chantelot, A.T. Hattersley, MODY group European Molecular Genetics Quality Network (EMQN).
Best practice guidelines for the molecular genetic diagnosis of maturity-onset diabetes of the young.
Diabetologia
2008 : Vol. 51, nr 4, s. 546-553, bibliogr. 46 poz., abstr.
p-ISSN: 0012-186X
AZ
ORG
AIF
IF: 6.418
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T[omasz] Klupa, I. Kowalska, K. Wyka, A.-M. Patch, J. Skupien, A. Noczynska, S. Ellard, A. Hattersley, J[acek] Sieradzki, W. Mlynarski, M[aciej] T. Malecki.
Variable clinical picture of mutations in the ABCC8 gene : can it be modified by the sensitivity to insulin or the islet-specific antibodies?
Diabetologia
2008 : Vol. 51 suppl. 1, s. S121, abstr. 280
44th Annual Meeting of the Euroean Association for the Study of Diabetes (EASD), Rome, 8-11 September, 2008.
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T[omasz] Klupa, A. Gach, A.-M. Patch, J. Skupien, J. PIetrzak, S. Ellard, A. Hattersley, W. Mlynarski, M[aciej] T. Malecki, J[acek] Sieradzki.
The prevalence estimation of PNDM in Poland : the relative contribution of mutation in KCNJ11 and ABCC8 genes.
Diabetologia
2007 : Vol. 50 suppl. 1, s. S124, abstr. 0281
43rd EASD Annual Meeting, Amsterdam, The Netherlands, 18-21 September 2007.
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T[omasz] Klupa, S. Flanagan, J[oanna] Nazim, S. Ellard, M. Ciechanowska, J[erzy] Starzyk, J[acek] Sieradzki, A.T. Hattersley, M[aciej] T. Malecki.
Kir6.2 mutations search in patients with permanent neonatal diabetes from a Polish population.
Diabetologia
2005 : Vol. 48 suppl. 1, s. A 112, abstr. 297
41st EASD Annual Meeting, Athens, Grece, 10-15 September 2005.
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T[omasz] Klupa, E.L. Edghill, J[oanna] Nazim, J[acek] Sieradzki, S. Ellard, A.T. Hattersley, M[aciej] T. Malecki.
The identification of a R201H mutation in KCNJ11, which encodes Kir6.2, and successful transfer to sustained-release sulphonylurea therapy in a subject with neonatal diabetes : evidence for heterogeneity of beta cell function among carriers of the R201H mutation.
Diabetologia
2005 : Vol. 48, nr 5, s. 1029-1031, il., bibliogr. 7 poz.
LR
AIF
IF: 5.337
Adres url:
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