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Duplex scanning replaces arteriography and operative exploration in the diagnosis of potential cervical vascular injury.
BACKGROUND The pursuit of a diagnosis is more aggressive in suspected cervical vascular injury than in extremity vascular proximity injury, since the complications of missing the neck injury mayExpand
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First case report of rare congenital adrenal insufficiency caused by mutations in the CYP11A1 gene in the Czech Republic
Abstract We characterized a case of congenital adrenal insufficiency caused by cholesterol side-chain cleavage enzyme (P450scc) deficiency. The patient presented after birth with cardiopulmonaryExpand
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FATCO syndrome--fibular aplasia, tibial campomelia and oligosyndactyly.
Joint Bone Spine - In Press.Proof corrected by the author Available online since mercredi 13 octobre 2010
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The presence of cariogenic and periodontal pathogens in the oral cavity of one-year-old infants delivered pre-term with very low birthweights: a case control study
BackgroundRecently, the dental literature has focused mainly on the microbial colonization of healthy full-term infants and their mothers or caretakers. However, oral microbial acquisition byExpand
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1030 Vitamin D and Other Parameters of Calcium and Phosphate Metabolism in Healthy Term Newborns After Birth
1030 Vitamin D and Other Parameters of Calcium and Phosphate Metabolism in Healthy Term Newborns After Birth
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General and oral health status of preterm one-year-old very low and extremely low birthweight infants (a cross - sectional study).
AIMS The aim of the present study was to evaluate the general and oral health status of a group of preterm one-year-old very low (VLBW) and extremely low birthweight (ELBW) infants and make aExpand
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[Has the pregnancy outcome of women with pregestational diabetes mellitus improved in ten years?].
INTRODUCTION In spite of progress in medicine, studies from a number of countries indicate steadily increased risk of perinatal morbidity and mortality in the offspring of diabetic mothers. No dataExpand
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First 2 cases with thiamine‐responsive megaloblastic anemia in the Czech Republic, a rare form of monogenic diabetes mellitus: a novel mutation in the thiamine transporter SLC19A2 gene—intron 1
Thiamine‐responsive megaloblastic anemia (TRMA) is a rare autosomal recessive disorder caused by mutations in the SLC19A2 gene. To date at least 43 mutations have been reported for the gene encodingExpand
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Fatco syndrome (fibular Aplasia, tibial campomelia and oligosyndactyly)
Joint Bone Spine - In Press.Proof corrected by the author Available online since mercredi 13 octobre 2010
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Onemocnění vyvolaná lidskými herpetickými viry
Humanni herpeticke viry (HHV) patři do celedi Herpesviridae (tab. 1). Jedna se o poměrně velke DNA viry (s průměrem kolem 200 nm) s kubickou symetrii virove kapsidy. HHV jsou ubikviterni, jejichExpand