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 Huebner

Showing results (61-70 of 115) with videos related to

Pageof 12
Sort By:
Journal of Pediatric Hematology/Oncology|February 24, 2001
Temporary response of localized intracranial mast cell sarcoma to combination chemotherapyP P Guenther, A Huebner, S B Sobottka, et al.
Endocrine Research|February 24, 2001
Triple A syndrome--clinical aspects and molecular geneticsA Huebner, S J Yoon, F Ozkinay, et al.
Annals of Neurology|March 7, 2014
Pathology of inherited manganese transporter deficiencyMirna Lechpammer, Michael S Clegg, Zukhrofi Muzar, et al.
Journal of Substance Abuse Treatment|July 14, 2021
Comparative outcomes for Black children served by the Sobriety Treatment and Recovery Teams program for families with parental substance abuse and child maltreatmentRuth A Huebner, Tina Willauer, Martin T Hall, et al.
Cell Death and Differentiation|September 1, 2012
Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary ciliaD Dai, L Li, A Huebner, et al.
Neurology|August 10, 2005
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndromeJ S Müller, R Stucka, S Neudecker, et al.
Chemical Communications (Cambridge, England)|March 16, 2007
Quantitative detection of protein expression in single cells using droplet microfluidicsA Huebner, M Srisa-Art, D Holt, et al.
Journal of Endocrinological Investigation|October 2, 2009
Upper and lower motor neuron involvement as presenting manifestation of Triple A syndromeM F Messina, M Autunno, K Koehler, et al.
Hormone Research|January 9, 2009
Autosomal dominant neurohypophyseal diabetes insipidus in two families. Molecular analysis of the vasopressin-neurophysin II gene and functional studies of three missense mutationsC M Hedrich, A Zachurzok-Buczynska, A Gawlik, et al.
Applied Clinical Informatics|March 1, 2023
Telemedicine Use across Medical Specialties and DiagnosesVivian Hsiao, Thevaa Chandereng, Jeffrey A Huebner, et al.
Pageof 12

Showing results (61-70 of 115) with videos related to

Sort By:
Pageof 12
Journal of Pediatric Hematology/Oncology|February 24, 2001
Temporary response of localized intracranial mast cell sarcoma to combination chemotherapyP P Guenther, A Huebner, S B Sobottka, et al.
Endocrine Research|February 24, 2001
Triple A syndrome--clinical aspects and molecular geneticsA Huebner, S J Yoon, F Ozkinay, et al.
Annals of Neurology|March 7, 2014
Pathology of inherited manganese transporter deficiencyMirna Lechpammer, Michael S Clegg, Zukhrofi Muzar, et al.
Journal of Substance Abuse Treatment|July 14, 2021
Comparative outcomes for Black children served by the Sobriety Treatment and Recovery Teams program for families with parental substance abuse and child maltreatmentRuth A Huebner, Tina Willauer, Martin T Hall, et al.
Cell Death and Differentiation|September 1, 2012
Planar cell polarity effector gene Intu regulates cell fate-specific differentiation of keratinocytes through the primary ciliaD Dai, L Li, A Huebner, et al.
Neurology|August 10, 2005
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndromeJ S Müller, R Stucka, S Neudecker, et al.
Chemical Communications (Cambridge, England)|March 16, 2007
Quantitative detection of protein expression in single cells using droplet microfluidicsA Huebner, M Srisa-Art, D Holt, et al.
Journal of Endocrinological Investigation|October 2, 2009
Upper and lower motor neuron involvement as presenting manifestation of Triple A syndromeM F Messina, M Autunno, K Koehler, et al.
Hormone Research|January 9, 2009
Autosomal dominant neurohypophyseal diabetes insipidus in two families. Molecular analysis of the vasopressin-neurophysin II gene and functional studies of three missense mutationsC M Hedrich, A Zachurzok-Buczynska, A Gawlik, et al.
Applied Clinical Informatics|March 1, 2023
Telemedicine Use across Medical Specialties and DiagnosesVivian Hsiao, Thevaa Chandereng, Jeffrey A Huebner, et al.
Pageof 12