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M Piccione

Showing results (21-30 of 47) with videos related to

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American Journal of Medical Genetics|September 6, 1996
Lymphoproliferative disorders in Sotos syndrome: observation of two casesG Corsello, M Giuffrè, A Carcione, et al.
Minerva Pediatrica|November 6, 2007
Neonatal presentation of Prader Willi sindrome. Personal recordsM C Maggio, M Corsello, M Piccione, et al.
The American Journal of Psychiatry|June 1, 1981
Evaluation and diagnosis of persistent insomniaF J Zorick, T Roth, K M Hartze, et al.
Minerva Pediatrica|May 1, 1988
[Down's syndrome with unusual karyotype: tandem duplication of chromosome 21]L Giuffrè, M Cammarata, G Corsello, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Epidemiological study of nonsyndromic hearing loss in Sicilian newbornsM Niceta, C Fabiano, P Sammarco, et al.
Life Sciences|January 1, 1993
Plasma natriuretic factor(s) in patients with intracranial disease, renal salt wasting and hyperuricosuriaJ K Maesaka, J Venkatesan, J M Piccione, et al.
Science (New York, N.Y.)|November 24, 2007
Shape and temperature memory of nanocomposites with broadened glass transitionPierre Miaudet, Alain Derré, Maryse Maugey, et al.
Acta Europaea Fertilitatis|November 1, 1989
Genetic factors of recurrent abortionsM Cammarata, G Corsello, M Marino, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 1, 1992
Abnormal urate transport in patients with intracranial diseaseJ K Maesaka, J Venkatesan, J M Piccione, et al.
European Journal of Pediatrics|February 9, 1999
Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L)G Corsello, P Bosco, F Calì, et al.
Pageof 5

Showing results (21-30 of 47) with videos related to

Sort By:
Pageof 5
American Journal of Medical Genetics|September 6, 1996
Lymphoproliferative disorders in Sotos syndrome: observation of two casesG Corsello, M Giuffrè, A Carcione, et al.
Minerva Pediatrica|November 6, 2007
Neonatal presentation of Prader Willi sindrome. Personal recordsM C Maggio, M Corsello, M Piccione, et al.
The American Journal of Psychiatry|June 1, 1981
Evaluation and diagnosis of persistent insomniaF J Zorick, T Roth, K M Hartze, et al.
Minerva Pediatrica|May 1, 1988
[Down's syndrome with unusual karyotype: tandem duplication of chromosome 21]L Giuffrè, M Cammarata, G Corsello, et al.
American Journal of Medical Genetics. Part A|June 15, 2007
Epidemiological study of nonsyndromic hearing loss in Sicilian newbornsM Niceta, C Fabiano, P Sammarco, et al.
Life Sciences|January 1, 1993
Plasma natriuretic factor(s) in patients with intracranial disease, renal salt wasting and hyperuricosuriaJ K Maesaka, J Venkatesan, J M Piccione, et al.
Science (New York, N.Y.)|November 24, 2007
Shape and temperature memory of nanocomposites with broadened glass transitionPierre Miaudet, Alain Derré, Maryse Maugey, et al.
Acta Europaea Fertilitatis|November 1, 1989
Genetic factors of recurrent abortionsM Cammarata, G Corsello, M Marino, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|January 1, 1992
Abnormal urate transport in patients with intracranial diseaseJ K Maesaka, J Venkatesan, J M Piccione, et al.
European Journal of Pediatrics|February 9, 1999
Maternal phenylketonuria in two Sicilian families identified by maternal blood phenylalanine level screening and identification of a new phenylalanine hydroxylase gene mutation (P407L)G Corsello, P Bosco, F Calì, et al.
Pageof 5