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Concolino

Showing results (121-130 of 347) with videos related to

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JIMD Reports|July 3, 2013
Chiari 1 malformation and holocord syringomyelia in hunter syndromeRenzo Manara, Daniela Concolino, Angelica Rampazzo, et al.
Clinical Chemistry and Laboratory Medicine|July 10, 2007
Genetic cystic fibrosis transmembrane regulator 4016insT D1152H compound heterozygosity and male infertility: an Italian case reportSandro Rocchetti, Concetta Santonocito, Paola Concolino, et al.
Inorganic Chemistry|January 16, 2003
Syntheses and structures of methyltris(pyrazolyl)silane complexes of the group 6 metalsE E Pullen, D Rabinovich, C D Incarvito, et al.
European Journal of Clinical Investigation|February 9, 2011
Modelling the resource implications of managing adults with Fabry disease in ItalyJulian F Guest, Daniela Concolino, Raffaele Di Vito, et al.
BMC Medical Genetics|July 24, 2009
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia formPaola Concolino, Enrica Mello, Angelo Minucci, et al.
Italian Journal of Pediatrics|September 10, 2013
Home treatment in paediatric patients with Hunter syndrome: the first Italian experienceFerdinando Ceravolo, Italia Mascaro, Simona Sestito, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 2006
A case of patient affected by hirsutism carrying the P482S CYP21 gene mutation associated with loss of heterozygosity (LOH)Paola Concolino, Cinzia Carrozza, Angelo Minucci, et al.
Journal of Inherited Metabolic Disease|April 22, 2008
Serum prolactin as a tool for the follow-up of treated DHPR-deficient patientsD Concolino, G Muzzi, M Rapsomaniki, et al.
Human Genetics|April 4, 2008
Novel human pathological mutations. Gene Symbol: CYP21A2. Disease: Non-classic 21-hydroxylase deficiencyPaola Concolino, Concetta Santonocito, Angelo Minucci, et al.
Pediatric Pulmonology|January 24, 2006
Is there a relationship between ELF free-IGF-1 levels and fibrotic process enhancement characterizing CLD development in neutropenic premature babies?Ettore Capoluongo, Paola Concolino, Bruno Giardina, et al.
Pageof 35

Showing results (121-130 of 347) with videos related to

Sort By:
Pageof 35
JIMD Reports|July 3, 2013
Chiari 1 malformation and holocord syringomyelia in hunter syndromeRenzo Manara, Daniela Concolino, Angelica Rampazzo, et al.
Clinical Chemistry and Laboratory Medicine|July 10, 2007
Genetic cystic fibrosis transmembrane regulator 4016insT D1152H compound heterozygosity and male infertility: an Italian case reportSandro Rocchetti, Concetta Santonocito, Paola Concolino, et al.
Inorganic Chemistry|January 16, 2003
Syntheses and structures of methyltris(pyrazolyl)silane complexes of the group 6 metalsE E Pullen, D Rabinovich, C D Incarvito, et al.
European Journal of Clinical Investigation|February 9, 2011
Modelling the resource implications of managing adults with Fabry disease in ItalyJulian F Guest, Daniela Concolino, Raffaele Di Vito, et al.
BMC Medical Genetics|July 24, 2009
A new CYP21A1P/CYP21A2 chimeric gene identified in an Italian woman suffering from classical congenital adrenal hyperplasia formPaola Concolino, Enrica Mello, Angelo Minucci, et al.
Italian Journal of Pediatrics|September 10, 2013
Home treatment in paediatric patients with Hunter syndrome: the first Italian experienceFerdinando Ceravolo, Italia Mascaro, Simona Sestito, et al.
Clinica Chimica Acta; International Journal of Clinical Chemistry|February 28, 2006
A case of patient affected by hirsutism carrying the P482S CYP21 gene mutation associated with loss of heterozygosity (LOH)Paola Concolino, Cinzia Carrozza, Angelo Minucci, et al.
Journal of Inherited Metabolic Disease|April 22, 2008
Serum prolactin as a tool for the follow-up of treated DHPR-deficient patientsD Concolino, G Muzzi, M Rapsomaniki, et al.
Human Genetics|April 4, 2008
Novel human pathological mutations. Gene Symbol: CYP21A2. Disease: Non-classic 21-hydroxylase deficiencyPaola Concolino, Concetta Santonocito, Angelo Minucci, et al.
Pediatric Pulmonology|January 24, 2006
Is there a relationship between ELF free-IGF-1 levels and fibrotic process enhancement characterizing CLD development in neutropenic premature babies?Ettore Capoluongo, Paola Concolino, Bruno Giardina, et al.
Pageof 35