Showing 1 - 15 results of 15 for search 'Maciej Hilczer', query time: 0.83s Refine Results
  1. 1
    Hipokalcemia z towarzyszącymi łagodnymi zaburzeniami odporności i zmianami w ośrodkowym układzie nerwowym – opis przypadku pierwotnej niedoczynności przytarczyc
    by Anna Krakowska, Maciej Hilczer, Marcin Tkaczyk
    Published 2011-10-01
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  2. 2
    Limited usefulness of the test of spontaneous growth hormone (GH) nocturnal secretion as a screening procedure in diagnosing GH deficiency in children with short stature
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  3. 3
    Changes in circadian rhythm of prolactin in short children are dependent on growth hormone secretion
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  4. 4
    Relationship between IGF-I Concentration and Metabolic Profile in Children with Growth Hormone Deficiency: The Influence of Children’s Nutritional State as well as the Ghrelin, Leptin, Adiponectin, and Resistin Serum Concentrations
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  5. 5
    Delayed Diagnosis of Congenital Combined Pituitary Hormone Deficiency including Severe Growth Hormone Deficiency in Children with Persistent Neonatal Hypoglycemia—Case Reports and Review
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  6. 6
    Significance of Direct Confirmation of Growth Hormone Insensitivity for the Diagnosis of Primary IGF-I Deficiency
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  7. 7
    Transient Isolated, Idiopathic Growth Hormone Deficiency—A Self-Limiting Pediatric Disease with Male Predominance or a Diagnosis Based on Uncertain Criteria? Lesson from 20 Years’ Real-World Experience with Retesting at One Center
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  8. 8
    The Variability of Vitamin D Concentrations in Short Children with Short Stature from Central Poland—The Effects of Insolation, Supplementation, and COVID-19 Pandemic Isolation
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  9. 9
    Frequency of oligosymptomatic gastrointestinal tract diseases and its relation to insulin-like growth factor I in idiopathic (non-GH-deficient) short stature children
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  10. 10
    Pre-treatment growth and IGF-I deficiency as main predictors of response to growth hormone therapy in neural models
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  11. 11
    ORIGINAL PAPER: <br> Endocrine disorders in children with craniopharyngiomas during the preoperative period
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  12. 12
    Karyotype Abnormalities in the X Chromosome Predict Response to the Growth Hormone Therapy in Turner Syndrome
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  13. 13
    The prevalence of hypothyroxinemia in premature newborns
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  14. 14
    Correlation of Genotype and Perinatal Period, Time of Diagnosis and Anthropometric Data before Commencement of Recombinant Human Growth Hormone Treatment in Polish Patients with Prader–Willi Syndrome
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  15. 15
    Effects of Recombinant Human Growth Hormone Treatment, Depending on the Therapy Start in Different Nutritional Phases in Paediatric Patients with Prader–Willi Syndrome: A Polish Multicentre Study
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