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C Migliori

Showing results (11-20 of 16) with videos related to

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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|April 3, 2004
[Pneumothorax during nasal-CPAP: a predictable complication?]C Migliori, A Campana, D Cattarelli, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1981
[Study of the transmission of the 21-hydroxylase deficiency through the hormonal screening and the HLA-typing (author's transl)]E Bartolotta, C Migliori, A Gabrielli, et al.
Minerva Pediatrica|May 1, 1993
[The Schönlein-Henoch syndrome with severe multisystemic involvement]M Bosio, A Ravelli, N Ruperto, et al.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.
Pageof 2

Showing results (11-20 of 16) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 16 results.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|April 3, 2004
[Pneumothorax during nasal-CPAP: a predictable complication?]C Migliori, A Campana, D Cattarelli, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1981
[Study of the transmission of the 21-hydroxylase deficiency through the hormonal screening and the HLA-typing (author's transl)]E Bartolotta, C Migliori, A Gabrielli, et al.
Minerva Pediatrica|May 1, 1993
[The Schönlein-Henoch syndrome with severe multisystemic involvement]M Bosio, A Ravelli, N Ruperto, et al.
Human Genetics|January 1, 1981
HLA genotypes and HLA-linked genetic markers in Italian patients with classical 21-hydroxylase deficiencyM S Pollack, M I New, G J O'Neill, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1980
Cryptic 21-hydroxylase deficiency in families of patients with classical congenital adrenal hyperplasiaL S Levine, B Dupont, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|December 1, 1981
Genetic and hormonal characterization of cryptic 21-hydroxylase deficiencyL S Levine, B Dupont, F Lorenzen, et al.
Pageof 2