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2. Nationwide observational study of paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) in the Czech Republic

4. Genetic Testing of Children With Familial Tall Stature: Is it Worth Doing?

9. Disease characteristics of MCT8 deficiency: an international, retrospective, multicentre cohort study

10. Adult height in children born small for gestational age (SGA) with persistent short stature (SGA-SS). Growth hormone treatment outcomes from data of the Czech countrywide REPAR database

11. Pubertal growth in children born small for gestational age (SGA) with persistent short stature (SGA-SS). Growth hormone treatment outcomes from data of the Czech countywide REPAR database

14. Effectiveness and safety of the tri-iodothyronine analogue Triac in children and adults with MCT8 deficiency: an international, single-arm, open-label, phase 2 trial

18. Analysis of children with familial short stature: who should be indicated for genetic testing?

20. SALL4 Phenotype in Four Generations of One Family: An Interplay of the Upper Limb, Kidneys, and the Pituitary.

21. Integrative Role of the SALL4 Gene: From Thalidomide Embryopathy to Genetic Defects of the Upper Limb, Internal Organs, Cerebral Midline, and Pituitary.

22. The Genetic Landscape of Children Born Small for Gestational Age with Persistent Short Stature.

26. Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us?

29. Epidemiological and clinical characteristics of paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 (PIMS-TS) in the Czech Republic

30. Inborn errors of OAS–RNase L in SARS-CoV-2–related multisystem inflammatory syndrome in children

35. Treatment Burden of Weekly Somatrogon vs Daily Somatropin in Children With Growth Hormone Deficiency: A Randomized Study

43. Clinical Characterization of Patients With Autosomal Dominant Short Stature due to Aggrecan Mutations

45. Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK

47. Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms

48. Plain language summary for the manuscript: Understanding the burden of weekly somatrogon injections compared with daily somatropin injections in children with growth hormone deficiency

50. Karyotyping of Lymphocytes and Epithelial Cells of Distinct Embryonic Origin Does Not Help to Predict the Turner Syndrome Features

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