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

Janusz Zimowski

Showing results (1-10 of 19) with videos related to

Pageof 2
Sort By:
Neurologia I Neurochirurgia Polska|May 8, 2013
Two mutations in one dystrophin geneJanusz Zimowski, Elżbieta Fidziańska, Mariola Holding, et al.
Neurologia I Neurochirurgia Polska|November 15, 2006
[Pseudodominant inheritance of spinal muscular atrophy--father and son suffering from SMA]Maria Jedrzejowska, Agnieszka Madej-Pilarczyk, Janusz Zimowski, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|June 7, 2013
Complex glycerol kinase deficiency - X-linked contiguous gene syndrome involving congenital adrenal hypoplasia, glycerol kinase deficiency, muscular Duchenne dystrophy and intellectual disability (IL1RAPL gene deletion)Beata Wikiera, Aleksandra Jakubiak, Janusz Zimowski, et al.
The Application of Clinical Genetics|May 23, 2022
Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor RetardationMagdalena Pasińska, Ewelina Łazarczyk, Anna Repczyńska, et al.
European Eating Disorders Review : the Journal of the Eating Disorders Association|August 7, 2019
Interaction between polymorphisms of the oxytocinergic system genes and emotion perception in inpatients with anorexia nervosaKatarzyna Kucharska, Emilia Kot, Katarzyna Biernacka, et al.
Medycyna Wieku Rozwojowego|April 29, 2005
[Prenatal diagnosis of spinal muscular atrophy (SMA) -- indications, restrictions, interpretation of results]Maria Jedrzejowska, Janusz Zimowski, Wojciech Wiszniewski, et al.
Neurologia I Neurochirurgia Polska|January 16, 2013
Hereditary form of prion disease in PolandJanusz Zimowski, Jerzy Kulczycki, Wanda Lojkowska, et al.
Orphanet Journal of Rare Diseases|March 25, 2021
Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophyAnna Lusakowska, Maria Jedrzejowska, Anna Kaminska, et al.
Acta Biochimica Polonica|March 17, 2009
Phenotype modifiers of spinal muscular atrophy: the number of SMN2 gene copies, deletion in the NAIP gene and probably gender influence the course of the diseaseMaria Jedrzejowska, Michał Milewski, Janusz Zimowski, et al.
Developmental Period Medicine|February 21, 2017
Co-incidence of Turner syndrome and Duchenne muscular dystrophy - an important problem for the clinicianEwa Kaczorowska, Janusz Zimowski, Monika Cichoń-Kotek, et al.
Pageof 2

Showing results (1-10 of 19) with videos related to

Sort By:
Pageof 2
Neurologia I Neurochirurgia Polska|May 8, 2013
Two mutations in one dystrophin geneJanusz Zimowski, Elżbieta Fidziańska, Mariola Holding, et al.
Neurologia I Neurochirurgia Polska|November 15, 2006
[Pseudodominant inheritance of spinal muscular atrophy--father and son suffering from SMA]Maria Jedrzejowska, Agnieszka Madej-Pilarczyk, Janusz Zimowski, et al.
Pediatric Endocrinology, Diabetes, and Metabolism|June 7, 2013
Complex glycerol kinase deficiency - X-linked contiguous gene syndrome involving congenital adrenal hypoplasia, glycerol kinase deficiency, muscular Duchenne dystrophy and intellectual disability (IL1RAPL gene deletion)Beata Wikiera, Aleksandra Jakubiak, Janusz Zimowski, et al.
The Application of Clinical Genetics|May 23, 2022
Clinical Importance of aCGH in Genetic Counselling of Children with Psychomotor RetardationMagdalena Pasińska, Ewelina Łazarczyk, Anna Repczyńska, et al.
European Eating Disorders Review : the Journal of the Eating Disorders Association|August 7, 2019
Interaction between polymorphisms of the oxytocinergic system genes and emotion perception in inpatients with anorexia nervosaKatarzyna Kucharska, Emilia Kot, Katarzyna Biernacka, et al.
Medycyna Wieku Rozwojowego|April 29, 2005
[Prenatal diagnosis of spinal muscular atrophy (SMA) -- indications, restrictions, interpretation of results]Maria Jedrzejowska, Janusz Zimowski, Wojciech Wiszniewski, et al.
Neurologia I Neurochirurgia Polska|January 16, 2013
Hereditary form of prion disease in PolandJanusz Zimowski, Jerzy Kulczycki, Wanda Lojkowska, et al.
Orphanet Journal of Rare Diseases|March 25, 2021
Observation of the natural course of type 3 spinal muscular atrophy: data from the polish registry of spinal muscular atrophyAnna Lusakowska, Maria Jedrzejowska, Anna Kaminska, et al.
Acta Biochimica Polonica|March 17, 2009
Phenotype modifiers of spinal muscular atrophy: the number of SMN2 gene copies, deletion in the NAIP gene and probably gender influence the course of the diseaseMaria Jedrzejowska, Michał Milewski, Janusz Zimowski, et al.
Developmental Period Medicine|February 21, 2017
Co-incidence of Turner syndrome and Duchenne muscular dystrophy - an important problem for the clinicianEwa Kaczorowska, Janusz Zimowski, Monika Cichoń-Kotek, et al.
Pageof 2