Publications by authors named "Beata Wikiera"

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Mixed Segmental Uniparental Disomy of Chromosome 15q11-q1 Coexists with Homozygous Variant in Gene in Child with Prader-Willi and Lodder-Merla Syndrome.
Tomasz Marczyk, Maria Libura, Beata Wikiera, Magdalena Góralska, Agnieszka Pollak

Genes (Basel)· June 2025

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Syndrome of Congenital Insulin Resistance Caused by a Novel Gene Mutation.
Aleksandra Rojek, Beata Wikiera, Anna Noczynska, Marek Niedziela

J Clin Res Pediatr Endocrinol· August 2023

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Difficulties in Interpreting IGF-1 Levels in Short Stature Children Born Small for Gestational Age (SGA) Treated with Recombinant Human Growth Hormone (rhGH) Based on Data from Six Clinical Centers in Poland.
Marta Glińska, Mieczysław Walczak, Beata Wikiera, Beata Pyrżak, Anna Majcher

J Clin Med· June 2023

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Silver-Russell syndrome and Turner syndrome in a girl with short stature treated with growth hormone - case report.
Beata Wikiera, Julita Nocoń-Bohusz, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· February 2023

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Weight gain in type 1 diabetes during the SARS-CoV-2 pandemic. Does lockdown affect the metabolic control of pediatric patients?
Agnieszka Zubkiewicz-Kucharska, Beata Wikiera, Anna Noczyńska

Front Endocrinol (Lausanne)· November 2022

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Response to Treatment with Recombinant Human Growth Hormone (rhGH) of Short Stature Children Born Too Small for Gestational Age (SGA) in Selected Centres in Poland.
Marta Glińska, Mieczysław Walczak, Beata Wikiera, Beata Pyrżak, Anna Majcher

J Clin Med· May 2022

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Soluble Klotho Is Decreased in Children With Type 1 Diabetes and Correlated With Metabolic Control.
Agnieszka Zubkiewicz-Kucharska, Beata Wikiera, Anna Noczyńska

Front Endocrinol (Lausanne)· February 2022

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Complex glycerol kinase deficiency - long-term follow-up of two patients.
Beata Wikiera, Aleksandra Jakubiak, Izabela Łaczmanska, Anna Noczyńska, Robert Śmigiel

Pediatr Endocrinol Diabetes Metab· November 2021

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Treatment of severe primary IGF-1 deficiency using rhIGF-1 preparation - first three years of Polish experience.
Elżbieta Petriczko, Tomasz Jackowski, Anita Horodnicka-Józwa, Beata Wikiera, Anna Noczyńska

Endokrynol Pol· July 2019

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Metabolic disorders in polycystic ovary syndrome.
Beata Wikiera, Agnieszka Zubkiewicz-Kucharska, Julita Nocoń-Bohusz, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· September 2018

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The assessment of skeletal status in young patients with Turner syndrome by 2 densitometric techniques: Phalangeal quantitative ultrasound and dual energy X-ray absorptiometry.
Beata Wikiera, Agata Mierzwicka, Aleksander Basiak, Jowita Halupczok-Żyła, Diana Jędrzejuk

Adv Clin Exp Med· June 2018

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[Klinefelter syndrome in a boy with symptoms of precocious puberty].
Jolanta Bieniasz, Beata Wikiera, Ewa Głąb, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· September 2017

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The Influence of GnRH Analog Therapy on Growth in Central Precocious Puberty.
Ewa Głąb, Beata Wikiera, Jolanta Bieniasz, Ewa Barg

Adv Clin Exp Med· June 2016

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LPL gene mutation as the cause of severe hypertriglyceridemia in the course of ketoacidosis in a patient with newly diagnosed type 1 diabetes mellitus.
Julita Nocoń-Bohusz, Beata Wikiera, Aleksander Basiak, Robert Śmigiel, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· February 2016

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The presence of eye defects in patients with Turner syndrome is irrespective of their karyotype.
Beata Wikiera, Malgorzata Mulak, Maria Koltowska-Haggstrom, Anna Noczynska

Clin Endocrinol (Oxf)· December 2015

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Multihormonal hypopituitarism, hypothyroidism and hypoparathyroidism in a 17-years-old girl with Diamond-Blackfan anemia and secondary hemochromatosis.
Ewa Głąb, Ewa Barg, Beata Wikiera, Jolanta Bieniasz

Pediatr Endocrinol Diabetes Metab· February 2015

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Ganglioneuroma in a patient with Turner syndrome.
Beata Wikiera, Julita Nocoń-Bohusz, Jan Godziński, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· February 2015

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Analysis of chosen polymorphisms in FoxP3 gene in children and adolescents with autoimmune thyroid diseases.
Artur Bossowski, Hanna Borysewicz-Sańczyk, Natalia Wawrusiewicz-Kurylonek, Aneta Zasim, Mieczysław Szalecki, Beata Wikiera

Autoimmunity· September 2014

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Complex glycerol kinase deficiency - X-linked contiguous gene syndrome involving congenital adrenal hypoplasia, glycerol kinase deficiency, muscular Duchenne dystrophy and intellectual disability (IL1RAPL gene deletion).
Beata Wikiera, Aleksandra Jakubiak, Janusz Zimowski, Anna Noczyńska, Robert Smigiel

Pediatr Endocrinol Diabetes Metab· November 2013

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[Thyroid ectopy - the presentation of four patients].
Beata Wikiera, Julita Nocoń-Bohusz, Wojciech Gawron, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· November 2013

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Thyroidectomy in children: changing trends and surgical strategies.
Maciej Bagłaj, Sylwester Gerus, Urszula Dorobisz, Tadeusz Lukieńczuk, Beata Wikiera

Adv Clin Exp Med· August 2013

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A two year observation of the process of applying recombinant IGF-1 to treat short stature in children with primary IGF-1 deficiency -- case reports of 3 patients.
Elżbieta Petriczko, Beata Wikiera, Anita Horodnicka-Józwa, Katarzyna Marcinkiewicz, Justyna Szmit-Domagalska

Pediatr Endocrinol Diabetes Metab· April 2012

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Coincidence of Poland's syndrome with Turner's syndrome.
Beata Wikiera, Elżbieta Wójcik, Andrzej Szuba, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· June 2011

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[Lipoprotein a (Lp(a)) in patients with Turner's syndrome].
Beata Wikiera, Jolanta Bieniasz, Ewa Barg, Ewa Głab, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· July 2010

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Sex chromosome pentasomy 49,XXXXY connected with hypothyroidism. Case report.
Beata Wikiera, Ewa Głab, Ryszard Slezak, Elzbieta Wójcik, Anna Noczyńska

Pediatr Endocrinol Diabetes Metab· October 2009

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