Plasma calcitonin in primary and secondary hyperparathyroidism

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The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.

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Histology and histopathology·2010

Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency.

Clinical genetics·2010

A new predictive index for vertebral fractures: the sum of the anterior vertebral body heights.

Bone·2009

Bone turnover, osteopenia and vascular calcifications in hemodialysis patients. A histomorphometric and multislice CT study.

American journal of nephrology·2008

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Israel journal of medical sciences·1998

Complementary medicine--a critical review.

Israel journal of medical sciences·1998

The Israel Longitudinal Mortality Study--differential mortality in Israel 1983-1992: objectives, materials, methods and preliminary results.

Israel journal of medical sciences·1998

Detection and typing of human papillomavirus DNAs by restriction endonuclease mapping of the PCR products.

Israel journal of medical sciences·1998

A comparison between arterial- and venous-sampled activated clotting time measurements.

Israel journal of medical sciences·1998

Heart rate variability in patients with secondary amyloidosis.

Israel journal of medical sciences·1998

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Molecular cancer research : MCR·2026

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Iranian journal of pathology·2026

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Two cases of giant cell tumours of the orbit: one case of giant cell tumor associated with Paget's disease of bone and one case of tenosynovial giant cell tumor.

Orbit (Amsterdam, Netherlands)·2026

Outcomes after surgical treatment of chest wall sarcomas.

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Plasma calcitonin in primary and secondary hyperparathyroidism

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PIXE technique for calcium analysis of human bone.

The Italian screening program for primary congenital hypothyroidism: actions to improve screening, diagnosis, follow-up, and surveillance.

Medial artery calcification of uremic patients: a histological, histochemical and ultrastructural study.

Phenotypic variability, neurological outcome and genetics background of 6-pyruvoyl-tetrahydropterin synthase deficiency.

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