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Janusz Zimowski

Showing results (11-20 of 19) with videos related to

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Neuroepidemiology|January 22, 2010
Incidence of spinal muscular atrophy in Poland--more frequent than predicted?Maria Jedrzejowska, Michal Milewski, Janusz Zimowski, et al.
Neurologia I Neurochirurgia Polska|May 5, 2005
Application of a rapid non-invasive technique in the molecular diagnosis of spinal muscular atrophy (SMA)Maria Jedrzejowska, Wojciech Wiszniewski, Janusz Zimowski, et al.
Neuro Endocrinology Letters|August 1, 2017
Genetic polymorphisms and serum concentrations of adiponectin and resistin in anorexia nervosa and healthy controls - pilot studyKarolina Ziora-Jakutowicz, Janusz Zimowski, Katarzyna T Ziora, et al.
European Journal of Human Genetics : EJHG|March 14, 2008
Unaffected patients with a homozygous absence of the SMN1 geneMaria Jedrzejowska, Janina Borkowska, Janusz Zimowski, et al.
Endokrynologia Polska|July 22, 2021
Evaluation of the frequency of RETN c.62G>A and RETN c.-180C>G polymorphisms in the resistin coding gene in girls with anorexia nervosaKarolina N Ziora-Jakutowicz, Janusz Zimowski, Katarzyna Ziora, et al.
Endokrynologia Polska|July 22, 2021
Evaluation of the frequency of ADIPOQ c.45 T>G and ADIPOQ c.276 G>T polymorphisms in adiponectin coding gene in girls with anorexia nervosaKarolina N Ziora-Jakutowicz, Janusz Zimowski, Katarzyna Ziora, et al.
Mitochondrion|May 31, 2013
The natural history of SCO2 deficiency in 36 Polish children confirmed the genotype-phenotype correlationEwa Pronicka, Dorota Piekutowska-Abramczuk, Tamara Szymańska-Dębińska, et al.
JIMD Reports|October 3, 2015
No Evidence for Association of SCO2 Heterozygosity with High-Grade Myopia or Other Diseases with Possible Mitochondrial DysfunctionDorota Piekutowska-Abramczuk, Beata Kocyła-Karczmarewicz, Maja Małkowska, et al.
Human Mutation|January 22, 2015
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutationsCatherine L Bladen, David Salgado, Soledad Monges, et al.
Pageof 2

Showing results (11-20 of 19) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 19 results.
Neuroepidemiology|January 22, 2010
Incidence of spinal muscular atrophy in Poland--more frequent than predicted?Maria Jedrzejowska, Michal Milewski, Janusz Zimowski, et al.
Neurologia I Neurochirurgia Polska|May 5, 2005
Application of a rapid non-invasive technique in the molecular diagnosis of spinal muscular atrophy (SMA)Maria Jedrzejowska, Wojciech Wiszniewski, Janusz Zimowski, et al.
Neuro Endocrinology Letters|August 1, 2017
Genetic polymorphisms and serum concentrations of adiponectin and resistin in anorexia nervosa and healthy controls - pilot studyKarolina Ziora-Jakutowicz, Janusz Zimowski, Katarzyna T Ziora, et al.
European Journal of Human Genetics : EJHG|March 14, 2008
Unaffected patients with a homozygous absence of the SMN1 geneMaria Jedrzejowska, Janina Borkowska, Janusz Zimowski, et al.
Endokrynologia Polska|July 22, 2021
Evaluation of the frequency of RETN c.62G>A and RETN c.-180C>G polymorphisms in the resistin coding gene in girls with anorexia nervosaKarolina N Ziora-Jakutowicz, Janusz Zimowski, Katarzyna Ziora, et al.
Endokrynologia Polska|July 22, 2021
Evaluation of the frequency of ADIPOQ c.45 T>G and ADIPOQ c.276 G>T polymorphisms in adiponectin coding gene in girls with anorexia nervosaKarolina N Ziora-Jakutowicz, Janusz Zimowski, Katarzyna Ziora, et al.
Mitochondrion|May 31, 2013
The natural history of SCO2 deficiency in 36 Polish children confirmed the genotype-phenotype correlationEwa Pronicka, Dorota Piekutowska-Abramczuk, Tamara Szymańska-Dębińska, et al.
JIMD Reports|October 3, 2015
No Evidence for Association of SCO2 Heterozygosity with High-Grade Myopia or Other Diseases with Possible Mitochondrial DysfunctionDorota Piekutowska-Abramczuk, Beata Kocyła-Karczmarewicz, Maja Małkowska, et al.
Human Mutation|January 22, 2015
The TREAT-NMD DMD Global Database: analysis of more than 7,000 Duchenne muscular dystrophy mutationsCatherine L Bladen, David Salgado, Soledad Monges, et al.
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