Early-onset pulmonary and cutaneous vasculitis driven by constitutively active SRC-family kinase HCK von Kanderova, Veronika, Svobodova, Tamara, Borna, Simon, Fejtkova, Martina, Martinu, Vendula, Paderova, Jana, Svaton, Michael, Kralova, Jarmila, Fronkova, Eva, Klocperk, Adam, Pruhova, Stepanka, Lee-Kirsch, Min Ae, Hornofova, Ludmila, Koblizek, Miroslav, Novak, Petr, Zimmermannova, Olga, Parackova, Zuzana, Sediva, Anna, Kalina, Tomas, Janda, Ales, Kayserova, Jana, Dvorakova, Marcela, Macek, Milan, Pohunek, Petr, Sedlacek, Petr, Poh, Ashleigh, Ernst, Matthias, Brdicka, Tomas, Hrusak, Ondrej, Lebl, Jan

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Blastocystis in the faeces of children from six distant countries: prevalence, quantity, subtypes and the relation to the gut bacteriome von Cinek, Ondrej, Polackova, Katerina, Odeh, Rasha, Alassaf, Abeer, Kramna, Lenka, Ibekwe, MaryAnn Ugochi, Majaliwa, Edna Siima, Ahmadov, Gunduz, Elmahi, Bashir Mukhtar Elwasila, Mekki, Hanan, Oikarinen, Sami, Lebl, Jan, Abdullah, Mohammed Ahmed

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Isolated growth hormone deficiency in children with vertically transmitted short stature: What do the genes tell us? von Plachy, Lukas, Amaratunga, Shenali Anne, Dusatkova, Petra, Maratova, Klara, Neuman, Vit, Petruzelkova, Lenka, Zemkova, Dana, Obermannova, Barbora, Snajderova, Marta, Kolouskova, Stanislava, Sumnik, Zdenek, Lebl, Jan, Pruhova, Stepanka

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Hepatic phenotypes of HNF1B gene mutations:A case of neonatal cholestasis requiring portoenterostomy and literature review von Kotalova, Radana, Dusatkova, Petra, Cinek, Ondrej, Dusatkova, Lenka, Dedic, Tomas, Seeman, Tomas, Lebl, Jan, Pruhova, Stepanka

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Haplotype analysis of the X chromosome in patients with Turner syndrome in order to verify the possible effect of imprinting on selected symptoms von Vrtel, Petr, Vrtel, Radek, Klaskova, Eva, Vrbicka, Dita, Adamova, Katerina, Pavlicek, Jan, Hana, Vaclav, Soucek, Ondrej, Stara, Veronika, Lebl, Jan, Snajdrova, Marta, Zapletalova, Jirina, Furst, Tomas, Kapralova, Sabina, Tauber, Zdenek, Krejcirikova, Eva, Routilova, Marketa, Stellmachova, Julia, Vodicka, Radek, Prochazka, Martin

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Etiology of combined pituitary hormone deficiency: GNAO1 as a novel candidate gene von Plachy, Lukas, Dusatkova, Petra, Maratova, Klara, Amaratunga, Shenali Anne, Zemkova, Dana, Neuman, Vit, Kolouskova, Stanislava, Obermannova, Barbora, Snajderova, Marta, Sumnik, Zdenek, Lebl, Jan, Pruhova, Stepanka

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Understanding the burden of weekly somatrogon injections compared with daily somatropin injections in children with growth hormone deficiency: a plain language summary of publicati... von Maniatis, Aristides K., Carakushansky, Mauri, Galcheva, Sonya, Prakasam, Gnanagurudasan, Fox, Larry A., Dankovcikova, Adriana, Loftus, Jane, Palladino, Andrew A., Resa, Maria de los Angeles, Taylor, Carrie Turich, Dattani, Mehul T., Lebl, Jan

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Analysis of children with familial short stature: who should be indicated for genetic testing? von Plachy, Lukas, Petruzelkova, Lenka, Dusatkova, Petra, Maratova, Klara, Zemkova, Dana, Elblova, Lenka, Neuman, Vit, Kolouskova, Stanislava, Obermannova, Barbora, Snajderova, Marta, Sumnik, Zdenek, Lebl, Jan, Pruhova, Stepanka

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Clinical presentation and management of childhood lipodystrophic syndromes von Lebl, Jan, Chiarelli, Francesco

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Long-term follow up of carbohydrate metabolism and adverse events after termination of Omnitrope® treatment in children born small for gestational age von Walczak, Mieczyslaw, Szalecki, Mieczyslaw, Horneff, Gerd, Lebl, Jan, Kalina-Faska, Barbara, Giemza, Tomasz, Moldovanu, Florentina, Nanu, Michaela, Zouater, Hichem

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Glucokinase diabetes in 103 families from a country-based study in the Czech Republic: geographically restricted distribution of two prevalent GCK mutations von Pruhova, Stepanka, Dusatkova, Petra, Sumnik, Zdenek, Kolouskova, Stanislava, Pedersen, Oluf, Hansen, Torben, Cinek, Ondrej, Lebl, Jan

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Two Cases of Diabetic Ketoacidosis in HNF1A-MODY Linked to Severe Dehydration von Pruhova, Stepanka, Dusatkova, Petra, Neumann, David, Hollay, Erik, Cinek, Ondrej, Lebl, Jan, Sumnik, Zdenek

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The occurrence of ocular diseases in patients with Turner syndrome von Brunnerova, Renata, Lebl, Jan

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Differential diagnosis in paediatric inflammatory multisystem syndrome temporally associated with SARS-CoV-2 von David, Jan, Lebl, Jan

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Further evidence that mutations in INS can be a rare cause of Maturity-Onset Diabetes of the Young (MODY) von Boesgaard, Trine W, Pruhova, Stepanka, Andersson, Ehm A, Cinek, Ondrej, Obermannova, Barbora, Lauenborg, Jeannet, Damm, Peter, Bergholdt, Regine, Pociot, Flemming, Pisinger, Charlotta, Barbetti, Fabrizio, Lebl, Jan, Pedersen, Oluf, Hansen, Torben

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GLP-1 analogues in therapy of obese adolescents. Early real-life experience with liraglutide treatment von Křenek Malíková, Jana, Lebl, Jan

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Association between Neuromedin U Gene Variants and Overweight and Obesity von Hainerová, Irena, Torekov, Signe S., Ek, Jakob, Finková, Marie, Borch-Johnsen, Knut, Jørgensen, Torben, Madsen, Ole D., Lebl, Jan, Hansen, Torben, Pedersen, Oluf

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Metabolic Impact of Growth Hormone Treatment in Short Children Born Small for Gestational Age von Lebl, Jan, Lebenthal, Yael, Kolouskova, Stanislava, Steensberg, Adam, Jøns, Kirsten, Kappelgaard, Anne-Marie, Ibáñez, Lourdes, Phillip, Moshe

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Thirty years since the leptin discovery: messenger of adipose tissue, regulator of eating behavior and a unique drug von Lebl, Jan, Dušátková, Petra, Křenek Malíková, Jana

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Impaired Growth during Childhood in Patients with Primary Ciliary Dyskinesia von Svobodová, Tamara, Djakow, Jana, Zemková, Daniela, Cipra, Adam, Pohunek, Petr, Lebl, Jan

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