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P Balestrazzi

Showing results (31-40 of 43) with videos related to

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Acta Endocrinologica|September 1, 1990
Pulsatile growth hormone release in Turner's syndrome and short normal childrenL Ghizzoni, A Lamborghini, M Ziveri, et al.
Human Genetics|April 1, 1996
Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphismsP Gasparini, L D'Agruma, G Pio de Cillis, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Oculo-auriculo-vertebral spectrum in Klinefelter syndromeL Garavelli, R Virdis, A Donadio, et al.
Thyroidology|December 1, 1990
Three years of experience of the congenital hypothyroidism National RegisterM Sorcini, M E Grandolfo, C Fazzini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1981
[Yersinia enterocolitica infection in thalassemia. Report of one case (author's transl)]P Balestrazzi, G Banchini, M G Menozzi, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1981
[Premature thelarche and precocious puberty. Clinical findings and endocrinological data useful for differential diagnosis]M Vanelli, S Bernasconi, N Caronna, et al.
L'Ateneo Parmense. Acta Bio-Medica : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1980
[Accidental poisoning in children. Epidemiological study and their prevention]M Vanelli, G L de Angelis, N Caronna, et al.
Annali Dell'Istituto Superiore Di Sanita|January 1, 1994
[Neonatal screening in congenital hypothyroidism in Italy. The National Registry]M Sorcini, C Fazzini, A Olivieri, et al.
Clinical Genetics|June 1, 1995
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variantA Grifa, M R Piemontese, S Melchionda, et al.
Annali Dell'Istituto Superiore Di Sanita|January 1, 1992
[National Register of congenital hypothyroidism]M Sorcini Carta, C Fazzini, A Olivieri, et al.
Pageof 5

Showing results (31-40 of 43) with videos related to

Sort By:
Pageof 5
Acta Endocrinologica|September 1, 1990
Pulsatile growth hormone release in Turner's syndrome and short normal childrenL Ghizzoni, A Lamborghini, M Ziveri, et al.
Human Genetics|April 1, 1996
Scanning the first part of the neurofibromatosis type 1 gene by RNA-SSCP: identification of three novel mutations and of two new polymorphismsP Gasparini, L D'Agruma, G Pio de Cillis, et al.
Genetic Counseling (Geneva, Switzerland)|November 5, 1999
Oculo-auriculo-vertebral spectrum in Klinefelter syndromeL Garavelli, R Virdis, A Donadio, et al.
Thyroidology|December 1, 1990
Three years of experience of the congenital hypothyroidism National RegisterM Sorcini, M E Grandolfo, C Fazzini, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|July 1, 1981
[Yersinia enterocolitica infection in thalassemia. Report of one case (author's transl)]P Balestrazzi, G Banchini, M G Menozzi, et al.
Acta Bio-Medica De L'Ateneo Parmense : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1981
[Premature thelarche and precocious puberty. Clinical findings and endocrinological data useful for differential diagnosis]M Vanelli, S Bernasconi, N Caronna, et al.
L'Ateneo Parmense. Acta Bio-Medica : Organo Della Societa Di Medicina E Scienze Naturali Di Parma|January 1, 1980
[Accidental poisoning in children. Epidemiological study and their prevention]M Vanelli, G L de Angelis, N Caronna, et al.
Annali Dell'Istituto Superiore Di Sanita|January 1, 1994
[Neonatal screening in congenital hypothyroidism in Italy. The National Registry]M Sorcini, C Fazzini, A Olivieri, et al.
Clinical Genetics|June 1, 1995
Screening of neurofibromatosis type 1 gene: identification of a large deletion and of an intronic variantA Grifa, M R Piemontese, S Melchionda, et al.
Annali Dell'Istituto Superiore Di Sanita|January 1, 1992
[National Register of congenital hypothyroidism]M Sorcini Carta, C Fazzini, A Olivieri, et al.
Pageof 5