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Incidence, Paris Classification, and Follow‐up in a Nationwide Incident Cohort of Pediatric Patients With Inflammatory Bowel Disease

Journal of pediatric gastroenterology and nutrition, 2013-11, Vol.57 (5), p.576-582

2013

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Pregnancy in women with cystic fibrosis: 14 case reports and literature review

Orvosi hetilap, 2021-07, Vol.162 (28), p.1129

2021

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The 8.1 ancestral MHC haplotype is associated with delayed onset of colonization in cystic fibrosis

International immunology, 2006-11, Vol.18 (11), p.1585-1590

2006

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Quality of life in Hungarian patients with cystic fibrosis

Orvosi hetilap, 2013-05, Vol.154 (20), p.784

2013

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Relationship of infant feeding on childhood obesity. A literature review

Orvosi hetilap, 2017-06, Vol.158 (24), p.938

2017

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Effect of treatment with gonadotropin releasing hormone analogues in girls with idiopathic central precocious puberty

Orvosi hetilap, 2012-03, Vol.153 (11), p.418

2012

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Baseline Characteristics and Disease Phenotype in Inflammatory Bowel Disease

Journal of pediatric gastroenterology and nutrition, 2016-01, Vol.62 (1), p.50-55

2016

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Prof. dr. László Velkey (1927-2010)

Orvosi hetilap, 2010-06, Vol.151 (26), p.1076

Sólyom, Enikô

2010

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Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndrome

Genomics (San Diego, Calif.), 2004-05, Vol.83 (5), p.883-892

2004

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Relationship between skin bacterial colonization and the occurrence of allergen-specific and non-allergen-specific antibodies in sera of children with atopic eczema/dermatitis syndrome

Acta dermato-venereologica, 2004-01, Vol.84 (1), p.32-36

2004

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Optimizing estrogen treatment in Turner syndrome

Orvosi hetilap, 2003-03, Vol.144 (12), p.563

2003

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Factors influencing quality of life and disease severity in Hungarian children and young adults with cystic fibrosis

Italian journal of pediatrics, 2014-06, Vol.40 (1), p.50-50, Article 50

2014

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Prevalence of celiac disease in Turner syndrome

Orvosi hetilap, 2006-06, Vol.147 (25), p.1185

2006

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Diagnostic yield of upper endoscopy in paediatric patients with Crohn's disease and ulcerative colitis. Subanalysis of the HUPIR registry

Journal of Crohn's and colitis, 2012-02, Vol.6 (1), p.86-94

2012

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Mixed gonadal dysgenesis associated with an isodicentric Y chromosome

Orvosi hetilap, 2007-08, Vol.148 (33), p.1567

2007

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Low mannose-binding lectin (MBL) is associated with paediatric inflammatory bowel diseases and ileal involvement in patients with Crohn disease

Journal of Crohn's and colitis, 2013-03, Vol.7 (2), p.134-141

2013

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Molecular Genetic Diagnostic Difficulties in Two Hungarian Gypsy Samples with Cystic Fibrosis

International journal of human genetics, 2002-03, Vol.2 (1), p.41-44

2002

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'DOT-17α-HYDROXYPROGESTERONE' RADIOIMMUNOASSAY FOR IDENTIFICATION OF CONGENITAL ADRENAL HYPERPLASIA IN YOUNG INFANTS

Acta Paediatrica, 1981-12, Vol.70 (6), p.913-917

1981

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Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome

American journal of medical genetics, 2002-05, Vol.109 (3), p.234-237

2002

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Twenty-one years of prospective incidence of childhood type 1 diabetes in Hungary - the rising trend continues (or peaks and highlands?)

Pediatric diabetes, 2012-02, Vol.13 (1), p.21-25

2012

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Incidence, Paris Classification, and Follow‐up in a Nationwide Incident Cohort of Pediatric Patients With Inflammatory Bowel Disease

Pregnancy in women with cystic fibrosis: 14 case reports and literature review

The 8.1 ancestral MHC haplotype is associated with delayed onset of colonization in cystic fibrosis

Quality of life in Hungarian patients with cystic fibrosis

Relationship of infant feeding on childhood obesity. A literature review

Effect of treatment with gonadotropin releasing hormone analogues in girls with idiopathic central precocious puberty

Baseline Characteristics and Disease Phenotype in Inflammatory Bowel Disease

Prof. dr. László Velkey (1927-2010)

Disruption of the PDGFB gene in a 1;22 translocation patient does not cause Costello syndrome

Relationship between skin bacterial colonization and the occurrence of allergen-specific and non-allergen-specific antibodies in sera of children with atopic eczema/dermatitis syndrome

Optimizing estrogen treatment in Turner syndrome

Factors influencing quality of life and disease severity in Hungarian children and young adults with cystic fibrosis

Prevalence of celiac disease in Turner syndrome

Diagnostic yield of upper endoscopy in paediatric patients with Crohn's disease and ulcerative colitis. Subanalysis of the HUPIR registry

Mixed gonadal dysgenesis associated with an isodicentric Y chromosome

Low mannose-binding lectin (MBL) is associated with paediatric inflammatory bowel diseases and ileal involvement in patients with Crohn disease

Molecular Genetic Diagnostic Difficulties in Two Hungarian Gypsy Samples with Cystic Fibrosis

'DOT-17α-HYDROXYPROGESTERONE' RADIOIMMUNOASSAY FOR IDENTIFICATION OF CONGENITAL ADRENAL HYPERPLASIA IN YOUNG INFANTS

Refinement and delineation of the breakpoint regions of a chromosome 1;22 translocation in a patient with Costello syndrome

Twenty-one years of prospective incidence of childhood type 1 diabetes in Hungary - the rising trend continues (or peaks and highlands?)

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