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C Castellan

Showing results (1-10 of 16) with videos related to

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La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1992
[Bone density in swimmers]G Radetti, S Frizzera, C Castellan, et al.
American Journal of Medical Genetics|April 24, 1999
Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromesM Riegel, C Castellan, D Balmer, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1991
[Monitoring the treatment of precocious puberty with a GnRH-analog (buserelin): comparison of the GnRH-test with nocturnal pulsatility of LH, testosterone and 17-beta-estradiol]G Radetti, B Pasquino, C Castellan, et al.
Hormone Research|January 1, 1993
Bone mineral density in children and adolescent females treated with high doses of L-thyroxineG Radetti, C Castellan, L Tatò, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: HMBS. Disease: Porphyria, acute intermittentElena Di Pierro, V Brancaleoni, F Stanzial, et al.
International Endodontic Journal|September 16, 2009
Polymerization stress, flow and dentine bond strength of two resin-based root canal sealersS F C Souza, A C Bombana, C Francci, et al.
Annals of Neurology|September 28, 1998
Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South TyrolC Klein, P P Pramstaller, C C Castellan, et al.
Clinical Genetics|April 11, 2012
An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the AlpsM Fanin, F Benedicenti, C Fritegotto, et al.
Journal of Medical Genetics|December 1, 1998
Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndromeK Merienne, S Jacquot, E Trivier, et al.
American Journal of Medical Genetics|January 16, 1995
Trisomy 2p: analysis of unusual phenotypic findingsI W Lurie, H G Ilyina, D B Gurevich, et al.
Pageof 2

Showing results (1-10 of 16) with videos related to

Sort By:
Pageof 2
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1992
[Bone density in swimmers]G Radetti, S Frizzera, C Castellan, et al.
American Journal of Medical Genetics|April 24, 1999
Terminal deletion, del(1)(p36.3), detected through screening for terminal deletions in patients with unclassified malformation syndromesM Riegel, C Castellan, D Balmer, et al.
La Pediatria Medica E Chirurgica : Medical and Surgical Pediatrics|September 1, 1991
[Monitoring the treatment of precocious puberty with a GnRH-analog (buserelin): comparison of the GnRH-test with nocturnal pulsatility of LH, testosterone and 17-beta-estradiol]G Radetti, B Pasquino, C Castellan, et al.
Hormone Research|January 1, 1993
Bone mineral density in children and adolescent females treated with high doses of L-thyroxineG Radetti, C Castellan, L Tatò, et al.
Human Genetics|August 21, 2009
Novel human pathological mutations. Gene symbol: HMBS. Disease: Porphyria, acute intermittentElena Di Pierro, V Brancaleoni, F Stanzial, et al.
International Endodontic Journal|September 16, 2009
Polymerization stress, flow and dentine bond strength of two resin-based root canal sealersS F C Souza, A C Bombana, C Francci, et al.
Annals of Neurology|September 28, 1998
Clinical and genetic evaluation of a family with a mixed dystonia phenotype from South TyrolC Klein, P P Pramstaller, C C Castellan, et al.
Clinical Genetics|April 11, 2012
An intronic mutation causes severe LGMD2A in a large inbred family belonging to a genetic isolate in the AlpsM Fanin, F Benedicenti, C Fritegotto, et al.
Journal of Medical Genetics|December 1, 1998
Rapid immunoblot and kinase assay tests for a syndromal form of X linked mental retardation: Coffin-Lowry syndromeK Merienne, S Jacquot, E Trivier, et al.
American Journal of Medical Genetics|January 16, 1995
Trisomy 2p: analysis of unusual phenotypic findingsI W Lurie, H G Ilyina, D B Gurevich, et al.
Pageof 2