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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 deficiency
M 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 hyperplasia
L 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 deficiency
L S Levine, B Dupont, F Lorenzen, et al.
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of 2
Search research articles
Search
Showing results (11-20 of 16) with videos related to
Sort By:
Page
of 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 deficiency
M 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 hyperplasia
L 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 deficiency
L S Levine, B Dupont, F Lorenzen, et al.
Page
of 2