Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

A P D'Adamo

Showing results (1-10 of 5) with videos related to

Pageof 1
Sort By:
Annals of Emergency Medicine|December 30, 1999
Ethnicity and analgesic practiceK H Todd, C Deaton, A P D'Adamo, et al.
The New England Journal of Medicine|August 31, 1978
Response of 1alpha,25-dihydroxyvitamin D3 to hypocalcemia in human subjectsJ P Bilezikian, R E Canfield, T P Jacobs, et al.
BMC Pediatrics|May 11, 2020
Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case reportD Nistico', F Guidolin, C O Navarra, et al.
Kidney International|March 22, 2001
Cystinuria type I: identification of eight new mutations in SLC3A1L Bisceglia, J Purroy, M Jiménez-Vidal, et al.
Human Molecular Genetics|February 7, 2001
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuriaM A Font, L Feliubadaló, X Estivill, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Annals of Emergency Medicine|December 30, 1999
Ethnicity and analgesic practiceK H Todd, C Deaton, A P D'Adamo, et al.
The New England Journal of Medicine|August 31, 1978
Response of 1alpha,25-dihydroxyvitamin D3 to hypocalcemia in human subjectsJ P Bilezikian, R E Canfield, T P Jacobs, et al.
BMC Pediatrics|May 11, 2020
Dental anomalies as a possible clue of 1p36 deletion syndrome due to germline mosaicism: a case reportD Nistico', F Guidolin, C O Navarra, et al.
Kidney International|March 22, 2001
Cystinuria type I: identification of eight new mutations in SLC3A1L Bisceglia, J Purroy, M Jiménez-Vidal, et al.
Human Molecular Genetics|February 7, 2001
Functional analysis of mutations in SLC7A9, and genotype-phenotype correlation in non-Type I cystinuriaM A Font, L Feliubadaló, X Estivill, et al.
Pageof 1