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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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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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Large diaphragmatic defect: are skeletal deformities preventable?

Pediatric surgery international, 2011-12, Vol.27 (12), p.1343-1349

2011

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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.109-114

2013

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Defect-diaphragmatic ratio: a new parameter for assessment of defect size in neonates with congenital diaphragmatic hernia

Pediatric surgery international, 2012-10, Vol.28 (10), p.971-976

2012

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Is there any relation between paternal age and sporadic cases of neurofibromatosis Von Recklinghausen type 1?

Fertility and sterility, 2009, Vol.92 (3), p.S199-S199

2009

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Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Journal of medical genetics, 2004-08, Vol.41 (8), p.629-633

2004

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Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

Thorax, 2005-04, Vol.60 (4), p.320-325

2005

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137 The end of a long-term outbreak with highly transmissible Burkholderia cenocepacia ST32

Journal of cystic fibrosis, 2011, Vol.10, p.S35-S35

2011

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Effect of early physiotherapy intervention in CF babies persists at least till 12 years of age

Journal of cystic fibrosis, 2010, Vol.9, p.S75-S75

2010

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Cystic fibrosis-related diabetes (CFRD) in the Czech Republic

Journal of cystic fibrosis, 2008-06, Vol.7, p.S84-S84

2008

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Is intestinal inflammation present in CF patients?

Journal of cystic fibrosis, 2008-06, Vol.7, p.S80-S80

2008

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Forty years isolation from W. Europe and its influence on the course of CF: an unwanted experiment

Journal of cystic fibrosis, 2008-06, Vol.7, p.S114-S114

2008

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19 Summary of the simultaneous IRT/PAP/ST+DNA and IRT/DNA/IRT newborn screening protocols in the Czech Republic

Journal of cystic fibrosis, 2011, Vol.10, p.S5-S5

2011

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Factors influencing the worsening of lung function between 16 and 18 years of age in Czech patients

Journal of cystic fibrosis, 2009, Vol.8, p.S59-S59

2009

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Czech Dysplasia Metatarsal Type

American journal of medical genetics, 2004-08, Vol.129A (1), p.87-91

2004

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Reference data for jumping mechanography in healthy children and adolescents aged 6-18 years

Journal of musculoskeletal & neuronal interactions, 2013-09, Vol.13 (3), p.297-311

2013

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Manual contact-stimulating physiotherapy: a very important part of chest physiotherapy in CF infants

Journal of cystic fibrosis, 2008-06, Vol.7, p.S74-S74

2008

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Clinical outcome and CF care costs justify the need of newborn screening

Journal of cystic fibrosis, 2008-06, Vol.7, p.S14-S14

2008

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Sexuality in CF patients in Czech Republic

Journal of cystic fibrosis, 2008-06, Vol.7, p.S109-S109

2008

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364 Newborn screening in the Czech Republic: an effective tool for early detection of CF

Journal of cystic fibrosis, 2007, Vol.6, p.S89-S89

2007

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148 Pseudomonas aeruginosa infection: utility of microbiological, PCR-based and serological techniques

Journal of cystic fibrosis, 2007, Vol.6, p.S36-S36

2007

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365 Cystic fibrosis newborn screening in the Czech Republic: overview of a pilot study

Journal of cystic fibrosis, 2007, Vol.6, p.S89-S89

2007

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356 Newborn screening (NBS) facilitates diagnosis of previously unrecognised CF in older siblings

Journal of cystic fibrosis, 2007, Vol.6, p.S87-S87

2007

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NPR2 Variants are frequent among children with familial short stature and respond well to growth hormone therapy

Yearbook of Paediatric Endocrinology, 2020-10

2020

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

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

Large diaphragmatic defect: are skeletal deformities preventable?

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

Defect-diaphragmatic ratio: a new parameter for assessment of defect size in neonates with congenital diaphragmatic hernia

Is there any relation between paternal age and sporadic cases of neurofibromatosis Von Recklinghausen type 1?

Polymorphisms in the mannose binding lectin gene affect the cystic fibrosis pulmonary phenotype

Association of tumour necrosis factor alpha variants with the CF pulmonary phenotype

137 The end of a long-term outbreak with highly transmissible Burkholderia cenocepacia ST32

Effect of early physiotherapy intervention in CF babies persists at least till 12 years of age

Cystic fibrosis-related diabetes (CFRD) in the Czech Republic

Is intestinal inflammation present in CF patients?

Forty years isolation from W. Europe and its influence on the course of CF: an unwanted experiment

19 Summary of the simultaneous IRT/PAP/ST+DNA and IRT/DNA/IRT newborn screening protocols in the Czech Republic

Factors influencing the worsening of lung function between 16 and 18 years of age in Czech patients

Czech Dysplasia Metatarsal Type

Reference data for jumping mechanography in healthy children and adolescents aged 6-18 years

Manual contact-stimulating physiotherapy: a very important part of chest physiotherapy in CF infants

Clinical outcome and CF care costs justify the need of newborn screening

Sexuality in CF patients in Czech Republic

364 Newborn screening in the Czech Republic: an effective tool for early detection of CF

148 Pseudomonas aeruginosa infection: utility of microbiological, PCR-based and serological techniques

365 Cystic fibrosis newborn screening in the Czech Republic: overview of a pilot study

356 Newborn screening (NBS) facilitates diagnosis of previously unrecognised CF in older siblings

NPR2 Variants are frequent among children with familial short stature and respond well to growth hormone therapy

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