W. Tangheroni

Schwartz-Jampel syndrome Clinical, electrophysiological and histopathological study of a severe variant

A. Cao, C. Cianchetti, L. Calisti, 1978, Journal of the Neurological Sciences.

Ultrastructural features of the muscle fibers in congenital hypothyroidism

A. Cao, W. Tangheroni, Z. Gori, 2004, Virchows Archiv A.

Characterization of platelet alkaline phosphatase in normal subjects and in trisomy 21 Down's syndrome patients.

W. Tangheroni, G. Coppa, S. De Virgiliis, 1971, Clinica chimica acta; international journal of clinical chemistry.

Leukocyte Alkaline Phosphatase Isoenzymes in Down’s Syndrome

W. Tangheroni, G. Coppa, A. Cao, 1971 .

Haemoglobin J Sardegna: α50 (CD 8) Histidine → Aspartic Acid

W. Tangheroni, H. Lehmann, E. Gallo, 1968, Nature.

A family of juvenile proximal spinal muscular atrophy with dominant inheritance.

A. Cao, L. Calisti, W. Tangheroni, 1976, Journal of medical genetics.

Multiple anomalies associated with an extra small metacentric chromosome: Modified Giemsa stain results

A. Cao, W. Tangheroni, M. Furbetta, 2004, Humangenetik.

[OBSERVATIONS ON THE PATHOLOGY OF RICKETS].

W. Tangheroni, G. Menichini, 1964, Minerva Pediatrica.

[Proteinuria caused by transfusion of blood from nephrotic to non-nephrotic individuals].

W. Tangheroni, A. Gentili, G. Gelli, 1954, Minerva medica.