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

S Kurtoğlu

Showing results (1-10 of 35) with videos related to

Pageof 4
Sort By:
The West Indian Medical Journal|July 2, 2002
Images and diagnoses. Multiple epiphyseal dysplasiaH Caksen, S Kurtoğlu
Journal of Endocrinological Investigation|June 12, 2015
Growth hormone insensitivity: diagnostic and therapeutic approachesS Kurtoğlu, N Hatipoglu
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Do not overlook Weismann-Netter syndrome in differential diagnosis of skeletal dysplasiasH Caksen, S Kurtoğlu
Genetic Counseling (Geneva, Switzerland)|February 12, 2002
Larsen syndrome associated with severe congenital hydrocephalusH Caksen, S Kurtoğlu
Acta Neurologica Belgica|March 10, 2001
A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardationH Caksen, S Kurtoğlu
The Turkish Journal of Pediatrics|April 1, 1995
Direct communication between pulmonary artery and left atriumT Okten, Y Okumuş, S Kurtoğlu
The Turkish Journal of Pediatrics|October 1, 1992
Analyses of serum vitamin D-binding protein, ceruloplasmin and copper levels in preterm infantsH Paşaoğlu, S Kurtoğlu, S Muhtaroğlu
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association|October 25, 2019
Does meal-time insulin dosing based on fat-protein counting give positive results in postprandial glycaemic profile after a high protein-fat meal in adolescents with type 1 diabetes: a randomised controlled trialN Kaya, S Kurtoğlu, H Gökmen Özel
The Turkish Journal of Pediatrics|April 1, 1989
Hypernatremia in two collodion babiesU Soyuer, S Kurtoğlu, E Aktaş, et al.
Genetic Counseling (Geneva, Switzerland)|February 12, 2002
An analysis of seven infants with Brachmann-de Lange syndrome, of whom two identical twin sistersH Caksen, S Kurtoğlu, Y Cesur, et al.
Pageof 4

Showing results (1-10 of 35) with videos related to

Sort By:
Pageof 4
The West Indian Medical Journal|July 2, 2002
Images and diagnoses. Multiple epiphyseal dysplasiaH Caksen, S Kurtoğlu
Journal of Endocrinological Investigation|June 12, 2015
Growth hormone insensitivity: diagnostic and therapeutic approachesS Kurtoğlu, N Hatipoglu
Genetic Counseling (Geneva, Switzerland)|April 16, 2004
Do not overlook Weismann-Netter syndrome in differential diagnosis of skeletal dysplasiasH Caksen, S Kurtoğlu
Genetic Counseling (Geneva, Switzerland)|February 12, 2002
Larsen syndrome associated with severe congenital hydrocephalusH Caksen, S Kurtoğlu
Acta Neurologica Belgica|March 10, 2001
A case of Adams-Oliver syndrome associated with acrania, microcephaly, hemiplegia, epilepsy, and mental retardationH Caksen, S Kurtoğlu
The Turkish Journal of Pediatrics|April 1, 1995
Direct communication between pulmonary artery and left atriumT Okten, Y Okumuş, S Kurtoğlu
The Turkish Journal of Pediatrics|October 1, 1992
Analyses of serum vitamin D-binding protein, ceruloplasmin and copper levels in preterm infantsH Paşaoğlu, S Kurtoğlu, S Muhtaroğlu
Journal of Human Nutrition and Dietetics : the Official Journal of the British Dietetic Association|October 25, 2019
Does meal-time insulin dosing based on fat-protein counting give positive results in postprandial glycaemic profile after a high protein-fat meal in adolescents with type 1 diabetes: a randomised controlled trialN Kaya, S Kurtoğlu, H Gökmen Özel
The Turkish Journal of Pediatrics|April 1, 1989
Hypernatremia in two collodion babiesU Soyuer, S Kurtoğlu, E Aktaş, et al.
Genetic Counseling (Geneva, Switzerland)|February 12, 2002
An analysis of seven infants with Brachmann-de Lange syndrome, of whom two identical twin sistersH Caksen, S Kurtoğlu, Y Cesur, et al.
Pageof 4