Search Results - "Paležac, Lidija"
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Delineation of PIGV mutation spectrum and associated phenotypes in hyperphosphatasia with mental retardation syndrome
Published in European journal of human genetics : EJHG (01-06-2014)“…Three different genes of the glycosylphosphatidylinositol anchor synthesis pathway, PIGV, PIGO, and PGAP2, have recently been implicated in…”
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Tu2014 LYMPHANGIOGRAPHY AS A DIAGNOSTIC AND THERAPEUTIC TOOL FOR PEDIATRIC PROTEIN-LOSING ENTEROPATHYL
Published in Gastroenterology (New York, N.Y. 1943) (01-05-2020)Get full text
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Human Adenovirus B3 Associated Colitis and Hemophagocytic Lymphohistiocytosis in 9-Year-old Previously Healthy Girl
Published in The Pediatric infectious disease journal (01-07-2024)Get full text
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4
SAT-294 A Case of Turner Syndrome with Ambiguous Genitalia
Published in Journal of the Endocrine Society (30-04-2019)“…Background: Turner syndrome is a common genetic condition caused by complete or partial absence of X chromosome. Often this condition is diagnosed prenatally…”
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Spinal cord compression caused by multiple spinal osteochondromas
Published in Wiener Klinische Wochenschrift (01-09-2008)Get full text
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