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

Mlynarski

Showing results (121-130 of 274) with videos related to

Pageof 28
Sort By:
International Journal of Environmental Research and Public Health|November 26, 2022
Predictors of Early Cardiac Implantable Electronic Device Lead Dislodgement in the ElderlyRafal Mlynarski, Agnieszka Mlynarska, Michal Joniec, et al.
Pediatric Diabetes|February 16, 2012
Ancestral mutations may cause a significant proportion of GCK-MODYPetra Dusatkova, Stepanka Pruhova, Maciej Borowiec, et al.
Clinical Genetics|November 1, 2011
Doubling the referral rate of monogenic diabetes through a nationwide information campaign--update on glucokinase gene mutations in a Polish cohortM Borowiec, W Fendler, K Antosik, et al.
Plos One|December 27, 2014
Central nervous system PET-CT imaging reveals regional impairments in pediatric patients with Wolfram syndromeAgnieszka Zmyslowska, Bogdan Malkowski, Wojciech Fendler, et al.
Molecular Cytogenetics|August 15, 2020
Novel <i>FANCA</i> mutation in the first fully-diagnosed patient with Fanconi anemia in Polish population - case reportAnna Repczynska, Agata Pastorczak, Katarzyna Babol-Pokora, et al.
Diabetologia|December 29, 2010
HbA(1c) levels in schoolchildren with type 1 diabetes are seasonally variable and dependent on weather conditionsB Mianowska, W Fendler, A Szadkowska, et al.
The Review of Diabetic Studies : RDS|May 12, 2007
Assessment of insulin sensitivity in adults with permanent neonatal diabetes mellitus due to mutations in the KCNJ11 gene encoding Kir6.2Jan Skupien, Maciej T Malecki, Wojciech Mlynarski, et al.
Familial Cancer|April 28, 2021
Ovarian carcinoma in children with constitutional mutation of SMARCA4: single-family report and literature reviewAgata Pastorczak, Karolina Krajewska, Zuzanna Urbanska, et al.
Experimental Oncology|March 21, 2009
Polymorphisms of the DNA base excision repair gene MUTYH in head and neck cancerT Sliwinski, L Markiewicz, P Rusin, et al.
Diabetes, Obesity & Metabolism|April 20, 2022
A randomized pharmacokinetic and pharmacodynamic trial of two regular human insulins demonstrates bioequivalence in type 1 diabetes and availability of biosimilar insulin may improve access to this medicationSérgio Vencio, Rafael Caiado-Vencio, Leonardo Ferreira Caixeta, et al.
Pageof 28

Showing results (121-130 of 274) with videos related to

Sort By:
Pageof 28
International Journal of Environmental Research and Public Health|November 26, 2022
Predictors of Early Cardiac Implantable Electronic Device Lead Dislodgement in the ElderlyRafal Mlynarski, Agnieszka Mlynarska, Michal Joniec, et al.
Pediatric Diabetes|February 16, 2012
Ancestral mutations may cause a significant proportion of GCK-MODYPetra Dusatkova, Stepanka Pruhova, Maciej Borowiec, et al.
Clinical Genetics|November 1, 2011
Doubling the referral rate of monogenic diabetes through a nationwide information campaign--update on glucokinase gene mutations in a Polish cohortM Borowiec, W Fendler, K Antosik, et al.
Plos One|December 27, 2014
Central nervous system PET-CT imaging reveals regional impairments in pediatric patients with Wolfram syndromeAgnieszka Zmyslowska, Bogdan Malkowski, Wojciech Fendler, et al.
Molecular Cytogenetics|August 15, 2020
Novel <i>FANCA</i> mutation in the first fully-diagnosed patient with Fanconi anemia in Polish population - case reportAnna Repczynska, Agata Pastorczak, Katarzyna Babol-Pokora, et al.
Diabetologia|December 29, 2010
HbA(1c) levels in schoolchildren with type 1 diabetes are seasonally variable and dependent on weather conditionsB Mianowska, W Fendler, A Szadkowska, et al.
The Review of Diabetic Studies : RDS|May 12, 2007
Assessment of insulin sensitivity in adults with permanent neonatal diabetes mellitus due to mutations in the KCNJ11 gene encoding Kir6.2Jan Skupien, Maciej T Malecki, Wojciech Mlynarski, et al.
Familial Cancer|April 28, 2021
Ovarian carcinoma in children with constitutional mutation of SMARCA4: single-family report and literature reviewAgata Pastorczak, Karolina Krajewska, Zuzanna Urbanska, et al.
Experimental Oncology|March 21, 2009
Polymorphisms of the DNA base excision repair gene MUTYH in head and neck cancerT Sliwinski, L Markiewicz, P Rusin, et al.
Diabetes, Obesity & Metabolism|April 20, 2022
A randomized pharmacokinetic and pharmacodynamic trial of two regular human insulins demonstrates bioequivalence in type 1 diabetes and availability of biosimilar insulin may improve access to this medicationSérgio Vencio, Rafael Caiado-Vencio, Leonardo Ferreira Caixeta, et al.
Pageof 28