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

E Jamroz

Showing results (11-20 of 18) with videos related to

Pageof 2
Sort By:
You have reached the last page of results.This site can display upto 18 results.
Neurologia I Neurochirurgia Polska|July 4, 2013
Magnetic resonance spectroscopy and molecular studies in ornithine transcarbamylase deficiency novel mutation c.802A>G in exon 8 (p.Met268Val)E Jamroz, J Paprocka, M Sokół, et al.
Neurologia I Neurochirurgia Polska|October 15, 1998
[Lyme disease in children]E Marszał, K Wojaczyńska-Stanek, B Szwed-Białozyt, et al.
Folia Neuropathologica|May 15, 2016
Pelizaeus-Merzbacher disease in patients with molecularly confirmed diagnosisH Mierzewska, E Jamroz, T Mazurczak, et al.
Journal of Child Neurology|June 27, 2000
Agenesis of corpus callosum: clinical description and etiologyE Marszał, E Jamroz, J Pilch, et al.
Neurologia I Neurochirurgia Polska|April 18, 2000
[Cerebral tumors as a cause of refractory epilepsy in children]E Marszał, E Jamroz, B Szwed-Białozyt, et al.
Neurologia I Neurochirurgia Polska|July 1, 1991
[Leigh disease in a 3-year-old girl]J Kałuza, M Krauze, E Marszał, et al.
Wiadomosci Lekarskie (Warsaw, Poland : 1960)|April 1, 1992
[Congenital toxoplasmosis in a 6-week-old infant]M Krauze, E Marszał, K Wojaczyńska-Stanek, et al.
Clinical Genetics|June 22, 2010
Do children with Adams-Oliver syndrome require endocrine follow-up? New information on the phenotype and managementM A Kalina, B Kalina-Faska, J Paprocka, et al.
Pageof 2

Showing results (11-20 of 18) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 18 results.
Neurologia I Neurochirurgia Polska|July 4, 2013
Magnetic resonance spectroscopy and molecular studies in ornithine transcarbamylase deficiency novel mutation c.802A>G in exon 8 (p.Met268Val)E Jamroz, J Paprocka, M Sokół, et al.
Neurologia I Neurochirurgia Polska|October 15, 1998
[Lyme disease in children]E Marszał, K Wojaczyńska-Stanek, B Szwed-Białozyt, et al.
Folia Neuropathologica|May 15, 2016
Pelizaeus-Merzbacher disease in patients with molecularly confirmed diagnosisH Mierzewska, E Jamroz, T Mazurczak, et al.
Journal of Child Neurology|June 27, 2000
Agenesis of corpus callosum: clinical description and etiologyE Marszał, E Jamroz, J Pilch, et al.
Neurologia I Neurochirurgia Polska|April 18, 2000
[Cerebral tumors as a cause of refractory epilepsy in children]E Marszał, E Jamroz, B Szwed-Białozyt, et al.
Neurologia I Neurochirurgia Polska|July 1, 1991
[Leigh disease in a 3-year-old girl]J Kałuza, M Krauze, E Marszał, et al.
Wiadomosci Lekarskie (Warsaw, Poland : 1960)|April 1, 1992
[Congenital toxoplasmosis in a 6-week-old infant]M Krauze, E Marszał, K Wojaczyńska-Stanek, et al.
Clinical Genetics|June 22, 2010
Do children with Adams-Oliver syndrome require endocrine follow-up? New information on the phenotype and managementM A Kalina, B Kalina-Faska, J Paprocka, et al.
Pageof 2