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Concolino

Showing results (71-80 of 347) with videos related to

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European Journal of Pediatrics|August 31, 2013
Myoglobinuria as first clinical sign of a primary alpha-sarcoglycanopathyFerdinando Ceravolo, Sonia Messina, Carmelo Rodolico, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 2, 2013
CYP21A2 p.E238 deletion as result of multiple microconversion events: a genetic study on an Italian congenital adrenal hyperplasia (CAH) familyPaola Concolino, Enrica Mello, Cecilia Zuppi, et al.
Gene|February 7, 2014
Comments to “A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency”Paola Concolino, Enrica Mello, Aurora Rossodivita, et al.
Clinical Neuropharmacology|January 1, 1984
Steroid receptors in the pathogenesis of chronic subdural hematomaG Concolino, R Giuffrè, G Margiotta, et al.
Journal of Clinical Medicine|July 9, 2022
Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase DeficiencyRosa Maria Paragliola, Alessia Perrucci, Laura Foca, et al.
Journal of Medical Genetics|February 25, 1998
Partial trisomy 1(q42-->qter): a new case with a mild phenotypeD Concolino, R Cinti, L Ferraro, et al.
European Journal of Pediatrics|October 1, 1995
Normal serum levels of vitamin B12 and folic acid in children with phenylketonuriaP Strisciuglio, D Concolino, M T Moricca, et al.
Journal of Steroid Biochemistry|May 1, 1978
Specific progesterone receptor in human renal cancerG Concolino, A Marocchi, R Tenaglia, et al.
Folia Endocrinologica|December 1, 1974
Mineralocorticoid effect of glycyrrhetinic acid in normal subjectsF Sparano, C Tosti-Croce, G Concolino, et al.
Human Mutation|February 22, 2002
Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathyGiovanni Cuda, Andrea Mussari, Daniela Concolino, et al.
Pageof 35

Showing results (71-80 of 347) with videos related to

Sort By:
Pageof 35
European Journal of Pediatrics|August 31, 2013
Myoglobinuria as first clinical sign of a primary alpha-sarcoglycanopathyFerdinando Ceravolo, Sonia Messina, Carmelo Rodolico, et al.
Diagnostic Molecular Pathology : the American Journal of Surgical Pathology, Part B|February 2, 2013
CYP21A2 p.E238 deletion as result of multiple microconversion events: a genetic study on an Italian congenital adrenal hyperplasia (CAH) familyPaola Concolino, Enrica Mello, Cecilia Zuppi, et al.
Gene|February 7, 2014
Comments to “A rational, non-radioactive strategy for the molecular diagnosis of congenital adrenal hyperplasia due to 21-hydroxylase deficiency”Paola Concolino, Enrica Mello, Aurora Rossodivita, et al.
Clinical Neuropharmacology|January 1, 1984
Steroid receptors in the pathogenesis of chronic subdural hematomaG Concolino, R Giuffrè, G Margiotta, et al.
Journal of Clinical Medicine|July 9, 2022
Prevalence of CAH-X Syndrome in Italian Patients with Congenital Adrenal Hyperplasia (CAH) Due to 21-Hydroxylase DeficiencyRosa Maria Paragliola, Alessia Perrucci, Laura Foca, et al.
Journal of Medical Genetics|February 25, 1998
Partial trisomy 1(q42-->qter): a new case with a mild phenotypeD Concolino, R Cinti, L Ferraro, et al.
European Journal of Pediatrics|October 1, 1995
Normal serum levels of vitamin B12 and folic acid in children with phenylketonuriaP Strisciuglio, D Concolino, M T Moricca, et al.
Journal of Steroid Biochemistry|May 1, 1978
Specific progesterone receptor in human renal cancerG Concolino, A Marocchi, R Tenaglia, et al.
Folia Endocrinologica|December 1, 1974
Mineralocorticoid effect of glycyrrhetinic acid in normal subjectsF Sparano, C Tosti-Croce, G Concolino, et al.
Human Mutation|February 22, 2002
Co-existence of frataxin and cardiac troponin T gene mutations in a child with Friedreich Ataxia and familial hypertrophic cardiomyopathyGiovanni Cuda, Andrea Mussari, Daniela Concolino, et al.
Pageof 35