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biomedicina slovenica |
re="Horm Res" : 36
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Grošelj Urh; Grošelj Blaž; Kovač Jernej; Hovnik Tinka; Trebušak-Podkrajšek Katarina; Battelino Tadej
Identification of the NLRP3 inflammasome polymorphisms associated with the development of type-1 diabetes and celiac disease
2011 ►
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Battelino Nina; Šebeštjen Miran; Keber Irena; Blagus Rok; Hovnik Tina; Bratina Nataša; Battelino Tadej
Endothelial nitric oxide synthase T(-786)C polymorphism in children and adolescents with type 1 diabetes and impaired endothelium-dependent dilatation
2011 ►
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Rajić VD; Zdravković D; Bogdanović R; Stajić N; Marjanović B
Schimke immuno-osseous dysplasia - a rare cause of short stature
2002 ►
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Rajić VD; Zdravković DS; Milovanović D; Djurićić S; Milenković T; Rasovic N; Bosnic S; Milickovic M
Malignant germ cell tumor of undescendent intraabdominal testis
2003 ►
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Philip Mosche; Battelino Tadej; Rodriguez Henry; Danne Thomas
Continuous insulin infusion treatment in the pediatric age group - consensus meeting
2007 ►
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Kotnik P; Debeljak M; Avbelj M; Hovnik T; Uršič-Bratina N; Kržišnik C; Battelino T
Lack of association of common allelic variants in the thyroglobulin gene with Hashimoto's thyroiditis in young subjects with type 1 diabetes
2010 ►
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Trebušak-Podkrajšek Katarina; Kisand Kai; Meager Anthony; Bratanič Nina; Peterson Paert; Battelino Tadej
Autoantibodies against type 1 interferones and Th17-related cytokines in APS-1 patients
2009 ►
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Kotnik Primož; Debeljak Maruša; Avbelj Magdalena; Hovnik Tinka; Uršič-Bratina Nataša; Kržišnik Ciril; Battelino Tadej
Common allelic variants in the thyroglobulin gene are not associated with autoimmune thyroid disease in children, adolescents and young adults with type 1 diabetes
2007 ►
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Milenković Tatjana; Zdravković Dragan; Djordjević Maja; Trebušak-Podkrajšek Katarina; Minić Predrag; Battelino Tadej
A novel AIRE gene mutation in an APS 1 patient with adrenal failure, hypoparathyroidism, ovarian failure, growth hormone deficiency, asthma and chronic otitis media with effusion
2007 ►
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Milenković Tatjana; Zdravković Dragan; Trebušak-Podkrajšek Katarina; Bratanič Nina; Battelino Tadej
Genotype variations with two novel mutations and clinical phenotype in APS-1 patients: a single center experience 1987-2007
2008 ►
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Hovnik Tinka; Uršič-Bratina Nataša; Bratanič Nina; Trebušak-Podkrajšek Katarina; Kržišnik Ciril; Battelino Tadej
MnSOD, GSTT1 and GSTM1 polymorphisms in association with diabetic retinopathy
2008 ►
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Zaletel K; Gaberšček S; Pirnat E; Hojker S
Thyroid hormone levels in untreated patients with Graves' disease correlate with the peak systolic
2007 ►
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Gaberšček S; Fister P; Zaletel K; Krhin B; Pirnat E; Geršak K; Hojker S
Grounds for thyroid volume changes during pregnancy and after delivery in an lodine sufficient area
2007 ►
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Battelino Tadej; Trebušak-Podkrajšek Katarina; Bratanič Nina; Kržišnik Ciril
AIRE-1 mRNA analyses - an additional level of APS-1 molecular diagnostics
2005 ►
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Avbelj Magdalena; Trebušak-Podkrajšek Katarina; Bratanič Nevenka; Kržišnik Ciril; Battelino Tadej
Two novel TPO gene mutations in congenital hypothyroidism
2005 ►
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Kotnik Primož; Širca-Čampa Andreja; Zupančič Mirjana; Štimec Matevž; Smole Katarina; Fidler-Mis Nataša; Battelino Tadej; Kržišnik Ciril
Urinary iodine concentration and goiter prevalence in Slowenian adolescents
2005 ►
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Battelino Tadej; Danne Thomas; Deiss Dorothy; Pankowska Ewa; Phillip Moshe
The PedPump survey: more than seven daily boluses and less basal insulin are associated with lower GlyHbA1c in 1086 chuildren with T1 DM from 17 countries
2005 ►
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Tubiana-Rufi Nadia; Deiss Dorothee; Bolinder Jan; Riveline Jean-Pierre; Battelino Tadej; Bosi Emanuele; Kerr David; Phillip Moshe
Evaluation of the Guardian RT continuous glucose monitoring system with real time glucose values and alarms in children with type 1 diabetes mellitus: a potential new tool to improve metabolic control
2005 ►
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Luczay Andrea; Torok Dora; Ferenczi Anna; Battelino Tadej; Majnik Judit; Sallai Agnes; Gacs Zsofia; Solyom Janos
The N363S polymorphism of the glucocorticoid receptor modifies the phenotype of congential adrenal hyperplasia: a pilot study
2005 ►
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Votava F; Toeroek D; Kovacs J; Moeslinger D; Solyom J; Priblincova Z; Battelino T; Lebl J; Frisch H
Estimation of the false negative rate in the new-born screening on congenital adrenal hyperplasia
2002 ►
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Battelino T; Trebušak K; Bratanič N; Žerjav-Tanšek M
A novel mutation in a patient with atypical presentation of autoimmune polyglandular syndrome type 1 (APS-1)
2002 ►
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Hargitai G; Slyom J; Battelino T; Lebl J; Pribilincova Z; Hauspie R; Kovacs J; Waldhauser F; Frisch H
Growth patterns and final height in congenital adrenal hyperplasia (CAH). Results of a multicenter study
2000 ►
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Žerjav-Tanšek M; Stopar M; Dolžan V; Breskvar K; Kržišnik C; Battelino T
Genotype-phenotype correlation in Slovenian patients with congenital adrenal hyperplasia
2000 ►
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Kovacs J; Votava F; Heinze G; Solyom J; Lebl J; Pribilincova Z; Frisch H; Battelino T; Waldhauser F
Lessons from congenital adrenal hyperplasia (CAH) management in middle-Europe during the last 30 years
2000 ►
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Battelino T; Trebušak K; Bratanič N; Repič-Lampret B; Kržišnik C
Phenotype-genotype correlation in Slovenian patients with autoimmune polyglandular syndrome type I (APS-I)
2000 ►
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Žerjav-Tanšek M; Kržišnik C; Battelino T
Clinical and biochemical indicators of partial growth hormone (GH) insensitivity
1999 ►
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Krude H; Tanšek M; Biebermann H; Huhne K; Battelino T; Grueters A
A new case of POMC mutation confirming the phenotype of POMC deficiency syndrome
1999 ►
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Battelino T; Trebušak-Podkrajšek K; Bratanič N; Kržišnik C
Clinical and molecular spectrum of Slovenian patients with APS-1
2003 ►
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Kotnik P; Battelino T; Frokiaer J; Nielsen S; Kržišnik C
Urinary aquaporin 2 excretion in patients with congenital nephrogenic diabetes insipidus
2003 ►
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Uršič-Bratina N; Rajer E; Radan I; Bratanič N; Kržišnik C; Battelino T
Nocturnal hypoglycemia after evening exercise in adolescents with T1D on MDI or CSII
2003 ►
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Frisch H; Waldhauser F; Lebl J; Solyom J; Hargitai G; Kovacs J; Pribilincova Z; Kržišnik C; Battelino T
Congenital adrenal hyperplasia: lessons from a multinational study
2002 ►
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Hargitai Gabor; Bratanič N; Dolžan V; Kržišnik C; Repič-Lampert B; Stopar M; Trebušak K; Uršič-Bratina N; Žerjav-Tanšek M
Growth patterns and final height in congenital adrenal hyperplasia due to classical 21-hydroxylase deficiency
2001 ►
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Hargitai Gabor; Solyom Janos; Battelino Tadej; Lebl Jan; Pribilincova Zuzanna; Hauspie Roland; Kovasc Joszef; Waldhauser Franz; Frisch Herwig
Growth patterns and final height in congenital adrenal hyperplasia due to classical 21-hydroxylase deficiency
2001 ►
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Saggese G; Ranke MB; Saenger P; Rosenfeld RG; Tanaka T; Chaussain JL; Savage MO; Kržišnik C
Diagnosis and treatment of growth hormone deficiency in children and adolescents: towards a consensus
1998 ►
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Ranke MB; Savage MO; Chatelain PG; Preece MA; Rosenfeld RG; Wilton P; Kržišnik C
Long-term treatment of growth hormone insensitivity syndrome with IGF-I
1999 ►
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Ranke MB; Savage MO; Chatelain PG; Preece MA; Rosenfeld RG; Blum WF; Wilton P; Kržišnik Ciril
Insulin-like growth factor 1 improves height in growth hormone insensitivity: two years' results
1995 ►
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