Author Details
Skalniak, Anna, Poland
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Vol 70, No 5 (2019) - Reviews — Postgraduate Education
Pituitary tumours in MEN1 syndrome — the new insight into the diagnosis and treatment
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Vol 71, No 6 (2020) - Clinical Vignette
Acromegaly and late-onset primary hyperparathyroidism in a female with a rare MEN1 gene variant of yet undetermined clinical significance (p.Val167Ala)
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Vol 72, No 4 (2021) - Clinical Vignette
A rare case of aggressive, hereditary paraganglioma associated with a pathogenic variant in SDHD
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Vol 74, No 1 (2023) - Original Paper
Whole-exome sequencing as a tool for searching for genetic background modifiers in MEN1 patients with neuroendocrine pancreatic tumours, including insulinomas
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