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The Closed Range Property for the ∂¯-Operator on Planar Domains

The Journal of geometric analysis, 2021-02, Vol.31 (2), p.1646-1670

2021

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Gonadal Pathology and Tumor Risk in Relation to Clinical Characteristics in Patients with 45,X/46,XY Mosaicism

The journal of clinical endocrinology and metabolism, 2011-07, Vol.96 (7), p.E1171-E1180

2011

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Tumor Risk in Disorders of Sex Development

Sexual Development, 2010-09, Vol.4 (4-5), p.259-269

2010

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Artificially low cortical bone mineral density in Turner syndrome is due to the partial volume effect

Osteoporosis international, 2015-03, Vol.26 (3), p.1213-1218

2015

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Novel glucokinase gene mutation in the first Macedonian family tested for MODY

Diabetes research and clinical practice, 2017-08, Vol.130, p.86-89

2017

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Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme

Diabetic medicine, 2016-12, Vol.33 (12), p.1712-1716

2016

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The dynamic changes of zinc transporter 8 autoantibodies in Czech children from the onset of Type 1 diabetes mellitus

Diabetic medicine, 2014-02, Vol.31 (2), p.165-171

2014

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Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius

The journal of clinical endocrinology and metabolism, 2013-07, Vol.98 (7), p.E1241-E1247

2013

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Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4α mutations in a large European collection

Diabetologia, 2005-05, Vol.48 (5), p.878-885

2005

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P06.12: Increased prevalence of bicuspid aortic valve in Turner syndrome links with karyotype: a crucial importance of detailed cardiovascular screening

Ultrasound in obstetrics & gynecology, 2016-09, Vol.48 (S1), p.184-185

2016

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Convexity of level lines of Martin functions and applications

Analysis and mathematical physics, 2019-03, Vol.9 (1), p.443-452

2019

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Treatment Options for Children with Monogenic Forms of Obesity

Nutrition and Growth, 2013-01, Vol.106, p.105-112

2013

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Boys with haemophilia have low trabecular bone mineral density and sarcopenia, but normal bone strength at the radius

Haemophilia : the official journal of the World Federation of Hemophilia, 2012-03, Vol.18 (2), p.222-228

2012

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Lack of PAX4 mutations in 53 Czech MODYX families

Diabetic medicine, 2010-12, Vol.27 (12), p.1459-1460

2010

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Homozygous carriers of the G allele of rs4664447 of the glucagon gene (GCG) are characterised by decreased fasting and stimulated levels of insulin, glucagon and glucagon-like peptide (GLP)-1

Diabetologia, 2011-11, Vol.54 (11), p.2820-2831

2011

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Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4α, GCK and HNF-1α

Diabetologia, 2003-02, Vol.46 (2), p.291-295

2003

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Bone geometry and volumetric bone density at the radius in patients with isolated SHOX deficiency

Experimental and clinical endocrinology & diabetes, 2013-02, Vol.121 (2), p.109

2013

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Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia

European journal of endocrinology, 2005-07, Vol.153 (1), p.99

2005

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45,X/46,X,psu dic(Y) Gonadal Dysgenesis: Influence of the Two Cell Lines on the Clinical Phenotype, Including Gonadal Histology

Sexual development, 2013-01, Vol.7 (6), p.282-288

2013

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Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents

European journal of pediatrics, 2006-07, Vol.165 (7), p.446-452

2006

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Clinical characterization of patients with autosomal dominant short stature due to aggrecan mutations

The journal of clinical endocrinology and metabolism, 2017-02, Vol.102 (2), p.460-469

2017

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Bone mineral density is low even in prepubertal girls with Turner syndrome: A pQCT study

Bone (New York, N.Y.), 2009-07, Vol.45, p.S77-S78

2009

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The contribution of X-chromosome genomic imprinting to the bicuspid aortic valve and aortic coarctation prevalence in women with Turner syndrome

European heart journal, 2020-11, Vol.41 (Supplement_2)

2020

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Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists

European journal of medical genetics, 2022-01, Vol.65 (1), p.104372-104372, Article 104372

2022

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Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey

European journal of medical genetics, 2022-01, Vol.65 (1), p.104404-104404, Article 104404

2022

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The Closed Range Property for the ∂¯-Operator on Planar Domains

Gonadal Pathology and Tumor Risk in Relation to Clinical Characteristics in Patients with 45,X/46,XY Mosaicism

Tumor Risk in Disorders of Sex Development

Artificially low cortical bone mineral density in Turner syndrome is due to the partial volume effect

Novel glucokinase gene mutation in the first Macedonian family tested for MODY

Substantial proportion of MODY among multiplex families participating in a Type 1 diabetes prediction programme

The dynamic changes of zinc transporter 8 autoantibodies in Czech children from the onset of Type 1 diabetes mellitus

Prepubertal Girls With Turner Syndrome and Children With Isolated SHOX Deficiency Have Similar Bone Geometry at the Radius

Molecular genetics and phenotypic characteristics of MODY caused by hepatocyte nuclear factor 4α mutations in a large European collection

P06.12: Increased prevalence of bicuspid aortic valve in Turner syndrome links with karyotype: a crucial importance of detailed cardiovascular screening

Convexity of level lines of Martin functions and applications

Treatment Options for Children with Monogenic Forms of Obesity

Boys with haemophilia have low trabecular bone mineral density and sarcopenia, but normal bone strength at the radius

Lack of PAX4 mutations in 53 Czech MODYX families

Homozygous carriers of the G allele of rs4664447 of the glucagon gene (GCG) are characterised by decreased fasting and stimulated levels of insulin, glucagon and glucagon-like peptide (GLP)-1

Genetic epidemiology of MODY in the Czech republic: new mutations in the MODY genes HNF-4α, GCK and HNF-1α

Bone geometry and volumetric bone density at the radius in patients with isolated SHOX deficiency

Mutational spectrum of steroid 21-hydroxylase and the genotype-phenotype association in Middle European patients with congenital adrenal hyperplasia

45,X/46,X,psu dic(Y) Gonadal Dysgenesis: Influence of the Two Cell Lines on the Clinical Phenotype, Including Gonadal Histology

Aetiological heterogeneity of asymptomatic hyperglycaemia in children and adolescents

Clinical characterization of patients with autosomal dominant short stature due to aggrecan mutations

Bone mineral density is low even in prepubertal girls with Turner syndrome: A pQCT study

The contribution of X-chromosome genomic imprinting to the bicuspid aortic valve and aortic coarctation prevalence in women with Turner syndrome

Management of cardiac aspects in children with Noonan syndrome – results from a European clinical practice survey among paediatric cardiologists

Management of growth failure and other endocrine aspects in patients with Noonan syndrome across Europe: A sub-analysis of a European clinical practice survey

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