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F Cottafava

Showing results (41-50 of 64) with videos related to

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Minerva Pediatrica|April 30, 1987
[Incontinentia pigmenti. Observations and research in 2 cases]D Bartoli, C Balagi, M Gramegna, et al.
Minerva Pediatrica|December 31, 1987
[Stickler's syndrome]C Balagi, S Nieri, C Prestandrea, et al.
International Journal of Clinical Pharmacology Research|January 1, 1986
Changes of immunological parameters during auranofin treatment in children affected with juvenile chronic arthritisF Fantini, F Cottafava, A Martini, et al.
Minerva Pediatrica|June 1, 1990
[Monosomy 7qter: 2 new cases of chromosomal pathology with aspecific disorders of pre- and post-natal development]M G Vianello, F Cottafava, D Bartoli, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Cytochrome c oxidase deficiency in three patients with Leigh's diseaseM Di Rocco, E Veneselli, M O Ciccone, et al.
Minerva Pediatrica|December 31, 1978
[Clinical and immunological study of a case of mixed connective tissue disease (MCTD) with onset in childhood]F Cottafava, M Bertolotto, S Brida di Priò, et al.
Minerva Pediatrica|June 1, 1991
[The Guillain-Barré syndrome. The clinico-electrophysiological correlations]M N Carlizzi, L D Lamba, G Ravera, et al.
BMJ (Clinical Research Ed.)|January 27, 1990
Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-)S Galiano, G F Gaetani, A Barabino, et al.
The Journal of Rheumatology|August 1, 1990
Clonal analysis of joint fluid T lymphocytes in patients with juvenile rheumatoid arthritisA F De Maria, M S Malnati, A Poggi, et al.
Minerva Pediatrica|June 30, 1985
[Hereditary spherocytosis. Cases from the Pediatric Clinic]F Cottafava, A Di Maio, P Tosca, et al.
Pageof 7

Showing results (41-50 of 64) with videos related to

Sort By:
Pageof 7
Minerva Pediatrica|April 30, 1987
[Incontinentia pigmenti. Observations and research in 2 cases]D Bartoli, C Balagi, M Gramegna, et al.
Minerva Pediatrica|December 31, 1987
[Stickler's syndrome]C Balagi, S Nieri, C Prestandrea, et al.
International Journal of Clinical Pharmacology Research|January 1, 1986
Changes of immunological parameters during auranofin treatment in children affected with juvenile chronic arthritisF Fantini, F Cottafava, A Martini, et al.
Minerva Pediatrica|June 1, 1990
[Monosomy 7qter: 2 new cases of chromosomal pathology with aspecific disorders of pre- and post-natal development]M G Vianello, F Cottafava, D Bartoli, et al.
Journal of Inherited Metabolic Disease|January 1, 1988
Cytochrome c oxidase deficiency in three patients with Leigh's diseaseM Di Rocco, E Veneselli, M O Ciccone, et al.
Minerva Pediatrica|December 31, 1978
[Clinical and immunological study of a case of mixed connective tissue disease (MCTD) with onset in childhood]F Cottafava, M Bertolotto, S Brida di Priò, et al.
Minerva Pediatrica|June 1, 1991
[The Guillain-Barré syndrome. The clinico-electrophysiological correlations]M N Carlizzi, L D Lamba, G Ravera, et al.
BMJ (Clinical Research Ed.)|January 27, 1990
Favism in the African type of glucose-6-phosphate dehydrogenase deficiency (A-)S Galiano, G F Gaetani, A Barabino, et al.
The Journal of Rheumatology|August 1, 1990
Clonal analysis of joint fluid T lymphocytes in patients with juvenile rheumatoid arthritisA F De Maria, M S Malnati, A Poggi, et al.
Minerva Pediatrica|June 30, 1985
[Hereditary spherocytosis. Cases from the Pediatric Clinic]F Cottafava, A Di Maio, P Tosca, et al.
Pageof 7