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S Einaudi

Showing results (1-10 of 20) with videos related to

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Archivio Italiano Di Urologia, Nefrologia, Andrologia : Organo Ufficiale Dell'Associazione Per La Ricerca in Urologia = Urological, Nephrological, and Andrological Sciences|March 1, 1990
[Diagnosis of ambiguous genitalia]C de Sanctis, S Einaudi, L De Sanctis
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Therapy of idiopathic thrombocytopenic purpura]G Fiandino, M Messina, M Amerio, et al.
Drugs Under Experimental and Clinical Research|January 1, 1987
L-asparaginase-induced coagulopathy in children with acute lymphoblastic leukaemiaR Miniero, P Saracco, S Einaudi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[The glucose-6-phosphate dehydrogenase/6-phosphogluconate dehydrogenase ratio in the identification of glucose-6-phosphate dehydrogenase heterozygosity]O David, S Einaudi, M G Vota, et al.
The Journal of Pediatric Endocrinology|April 1, 1993
Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS Einaudi, R Lala, A Corrias, et al.
The Journal of Pediatric Endocrinology|October 1, 1994
HLA haplotypes and hormonal studies in 25 Italian families of patients with classical and non-classical 21-OH deficiencyS Einaudi, I Borelli, R Lala, et al.
Human Mutation|February 5, 2000
T426I a new mutation in the thyroid hormone receptor beta gene in a sporadic patient with resistance to thyroid hormone and dysmorphism. Mutations in brief no. 192. OnlineC Menzaghi, R Di Paola, A Corrias, et al.
Journal of Endocrinological Investigation|March 5, 2021
POR polymorphisms are associated with 21 hydroxylase deficiencyF Pecori Giraldi, S Einaudi, A Sesta, et al.
Journal of Endocrinological Investigation|July 31, 2010
Correlation between genotype and hormonal levels in heterozygous mutation carriers and non-carriers of 21-hydroxylase deficiencyE Napolitano, C Manieri, F Restivo, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 28, 2011
Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disordersA Mussa, F Porta, G Baldassarre, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Archivio Italiano Di Urologia, Nefrologia, Andrologia : Organo Ufficiale Dell'Associazione Per La Ricerca in Urologia = Urological, Nephrological, and Andrological Sciences|March 1, 1990
[Diagnosis of ambiguous genitalia]C de Sanctis, S Einaudi, L De Sanctis
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[Therapy of idiopathic thrombocytopenic purpura]G Fiandino, M Messina, M Amerio, et al.
Drugs Under Experimental and Clinical Research|January 1, 1987
L-asparaginase-induced coagulopathy in children with acute lymphoblastic leukaemiaR Miniero, P Saracco, S Einaudi, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|January 1, 1986
[The glucose-6-phosphate dehydrogenase/6-phosphogluconate dehydrogenase ratio in the identification of glucose-6-phosphate dehydrogenase heterozygosity]O David, S Einaudi, M G Vota, et al.
The Journal of Pediatric Endocrinology|April 1, 1993
Auxological and biochemical parameters in assessing treatment of infants and toddlers with congenital adrenal hyperplasia due to 21-hydroxylase deficiencyS Einaudi, R Lala, A Corrias, et al.
The Journal of Pediatric Endocrinology|October 1, 1994
HLA haplotypes and hormonal studies in 25 Italian families of patients with classical and non-classical 21-OH deficiencyS Einaudi, I Borelli, R Lala, et al.
Human Mutation|February 5, 2000
T426I a new mutation in the thyroid hormone receptor beta gene in a sporadic patient with resistance to thyroid hormone and dysmorphism. Mutations in brief no. 192. OnlineC Menzaghi, R Di Paola, A Corrias, et al.
Journal of Endocrinological Investigation|March 5, 2021
POR polymorphisms are associated with 21 hydroxylase deficiencyF Pecori Giraldi, S Einaudi, A Sesta, et al.
Journal of Endocrinological Investigation|July 31, 2010
Correlation between genotype and hormonal levels in heterozygous mutation carriers and non-carriers of 21-hydroxylase deficiencyE Napolitano, C Manieri, F Restivo, et al.
Osteoporosis International : a Journal Established As Result of Cooperation Between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA|September 28, 2011
Phalangeal quantitative ultrasound in 1,719 children and adolescents with bone disordersA Mussa, F Porta, G Baldassarre, et al.
Pageof 2