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	1.	For Debate: Should Bariatric Surgery be Performed in Children and Adolescents with Hypothalamic Obesity? [electronic resource] by Stolbova, Sarka Benes, Marek Petruzelkova, Lenka Lebl, Jan Kolouskova, Stanislava Producer: 20180226 In: Pediatric endocrinology reviews : PER vol. 14 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	2.	The cytokine production of peripheral blood mononuclear cells reflects the autoantibody profile of patients suffering from type 1 diabetes. [electronic resource] by Labikova, Jana Vcelakova, Jana Ulmannova, Tereza Petruzelkova, Lenka Kolouskova, Stanislava Stechova, Katerina Producer: 20150910 In: Cytokine vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	3.	Glucokinase Gene May Be a More Suitable Target Than the Insulin Gene for Detection of β Cell Death. [electronic resource] by Sklenarova, Jana Petruzelkova, Lenka Kolouskova, Stanislava Lebl, Jan Sumnik, Zdenek Cinek, Ondrej Producer: 20170929 In: Endocrinology vol. 158 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	4.	HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes. [electronic resource] by Dusatkova, Petra Pruhova, Stepanka Sumnik, Zdenek Kolouskova, Stanislava Obermannova, Barbora Cinek, Ondrej Lebl, Jan Producer: 20110705 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	5.	[Overgrowth in children and in adults: novel clinical view, novel genes, novel phenotypes]. [electronic resource] by Lebl, Jan Plachý, Lukáš Bláhová, Květa Elblová, Lenka Fencl, Filip Koloušková, Stanislava Průhová, Štěpánka Producer: 20190408 In: Casopis lekaru ceskych vol. 156 Availability: No items available. Save to lists Add to cart (remove)
	6.	No independent role of the -1123 G>C and+2740 A>G variants in the association of PTPN22 with type 1 diabetes and juvenile idiopathic arthritis in two Caucasian populations. [electronic resource] by Cinek, Ondrej Hradsky, Ondrej Ahmedov, Gunduz Slavcev, Antonij Kolouskova, Stanislava Kulich, Michal Sumnik, Zdenek Producer: 20070820 In: Diabetes research and clinical practice vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	7.	Low-dose insulin therapy in patients with cystic fibrosis and early-stage insulinopenia prevents deterioration of lung function: a 3-year prospective study. [electronic resource] by Koloušková, Stanislava Zemková, Daniela Bartošová, Jana Skalická, Veronika Šumník, Zdenĕk Vávrová, Vĕra Lebl, Jan Producer: 20111024 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 24 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	8.	HNF1A mutation presenting with fetal macrosomia and hypoglycemia in childhood prior to onset of overt diabetes. [electronic resource] by Dusátková, Petra Průhová, Stepánka Sumník, Zdenek Kolousková, Stanislava Obermannová, Barbora Cinek, Ondrej Lebl, Jan Producer: 20110830 In: Journal of pediatric endocrinology & metabolism : JPEM vol. 24 Availability: No items available. Save to lists Add to cart (remove)
	9.	High prevalence of coeliac disease in siblings of children with type 1 diabetes. [electronic resource] by Sumnik, Zdenek Kolouskova, Stanislava Malcova, Hana Vavrinec, Jan Venhacova, Jitrenka Lebl, Jan Cinek, Ondrej Producer: 20050412 In: European journal of pediatrics vol. 164 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	10.	Identification of CYP21A2 mutant alleles in Czech patients with 21-hydroxylase deficiency. [electronic resource] by Vrzalová, Zuzana Hrubá, Zuzana St'ahlová Hrabincová, Eva Pouchlá, Slavka Votava, Felix Kolousková, Stanislava Fajkusová, Lenka Producer: 20110110 In: International journal of molecular medicine vol. 26 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	11.	Chimeric CYP21A1P/CYP21A2 genes identified in Czech patients with congenital adrenal hyperplasia. [electronic resource] by Vrzalová, Zuzana Hrubá, Zuzana Hrabincová, Eva Sťahlová Vrábelová, Slávka Votava, Felix Koloušková, Stanislava Fajkusová, Lenka Producer: 20110804 In: European journal of medical genetics vol. 54 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	12.	NEUROD polymorphism Ala45Thr is associated with Type 1 diabetes mellitus in Czech children. [electronic resource] by Cinek, Ondrej Drevínek, Pavel Sumník, Zdenĕk Bendlová, Bĕla Sedláková, Pavlína Kolousková, Stanislava Snajderová, Marta Vavrinec, Jan Producer: 20031029 In: Diabetes research and clinical practice vol. 60 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	13.	Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations. [electronic resource] by Pruhova, Stepanka Dusatkova, Petra Sumnik, Zdenek Kolouskova, Stanislava Pedersen, Oluf Hansen, Torben Cinek, Ondrej Lebl, Jan Producer: 20110311 In: Pediatric diabetes vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	14.	Muscle function in Turner syndrome: normal force but decreased power. [electronic resource] by Soucek, Ondrej Lebl, Jan Matyskova, Jana Snajderova, Marta Kolouskova, Stanislava Pruhova, Stepanka Hlavka, Zdenek Sumnik, Zdenek Producer: 20151117 In: Clinical endocrinology vol. 82 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	15.	Metabolic impact of growth hormone treatment in short children born small for gestational age. [electronic resource] by Lebl, Jan Lebenthal, Yael Kolouskova, Stanislava Steensberg, Adam Jøns, Kirsten Kappelgaard, Anne-Marie Ibáñez, Lourdes Phillip, Moshe Producer: 20120213 In: Hormone research in paediatrics vol. 76 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	16.	Decreased dendritic cell numbers but increased TLR9-mediated interferon-alpha production in first degree relatives of type 1 diabetes patients. [electronic resource] by Kayserova, Jana Vcelakova, Jana Stechova, Katerina Dudkova, Eva Hromadkova, Hana Sumnik, Zdenek Kolouskova, Stanislava Spisek, Radek Sediva, Anna Producer: 20140912 In: Clinical immunology (Orlando, Fla.) vol. 153 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	17.	Muscle functions and bone strength are impaired in adolescents with type 1 diabetes. [electronic resource] by Maratova, Klara Soucek, Ondrej Matyskova, Jana Hlavka, Zdenek Petruzelkova, Lenka Obermannova, Barbora Pruhova, Stepanka Kolouskova, Stanislava Sumnik, Zdenek Producer: 20180702 In: Bone vol. 106 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	18.	Growth data in large series of 587 children and adolescents with type 1 diabetes mellitus. [electronic resource] by Lebl, Jan Schober, Edith Zidek, Thomas Baldis, Susana Rami, Birgit Pruhova, Stepanka Kolouskova, Stanislava Snajderova, Marta Frisch, Herwig Producer: 20040720 In: Endocrine regulations vol. 37 Availability: No items available. Save to lists Add to cart (remove)
	19.	Bone geometry and volumetric bone mineral density in girls with Turner syndrome of different pubertal stages. [electronic resource] by Soucek, Ondrej Lebl, Jan Snajderova, Marta Kolouskova, Stanislava Rocek, Miloslav Hlavka, Zdenek Cinek, Ondrej Rittweger, Joern Sumnik, Zdenek Producer: 20110801 In: Clinical endocrinology vol. 74 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	20.	Unusually severe phenotype of neonatal primary hyperparathyroidism due to a heterozygous inactivating mutation in the CASR gene. [electronic resource] by Obermannova, Barbora Banghova, Karolina Sumník, Zdenek Dvorakova, Hana M Betka, Jan Fencl, Filip Kolouskova, Stanislava Cinek, Ondrej Lebl, Jan Producer: 20090727 In: European journal of pediatrics vol. 168 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)

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Your search returned 40 results.