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O Hurko

Showing results (41-50 of 58) with videos related to

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American Journal of Human Genetics|September 1, 1996
Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritanceJ T Walkup, M C LaBuda, H S Singer, et al.
Journal of Medical Genetics|September 9, 2000
Achondroplasia and nail-patella syndrome: the compound phenotypeM J Wright, M C Ain, M V Clough, et al.
The Journal of Pediatrics|May 15, 1998
Sleep-disordered breathing in children with achondroplasiaP J Mogayzel, J L Carroll, G M Loughlin, et al.
Journal of Neurosurgical Anesthesiology|July 25, 2000
Perioperative intracranial hemorrhage in achondroplasia: a case reportI Elmaci, M C Ain, M J Wright, et al.
AJNR. American Journal of Neuroradiology|March 1, 1992
Chromosomal disorders: background and neuroradiologyA J Kumar, T P Naidich, G Stetten, et al.
Neurology|March 1, 1997
Linkage of the locus for cerebral cavernous hemangiomas to human chromosome 7q in four families of Mexican-American descentM H Polymeropoulos, O Hurko, F Hsu, et al.
The Journal of Clinical Investigation|February 1, 1988
Oral carnitine therapy in children with cystinosis and renal Fanconi syndromeW A Gahl, I Bernardini, M Dalakas, et al.
AJNR. American Journal of Neuroradiology|May 1, 1995
Reversibility of white matter changes and dementia after treatment of dural fistulasS M Zeidman, L H Monsein, O Arosarena, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1992
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcriptsA Chomyn, A Martinuzzi, M Yoneda, et al.
Basic Life Sciences|January 1, 1988
Cervicomedullary cord compression in young children with achondroplasia: value of comprehensive neurologic and respiratory evaluationC S Reid, R E Pyeritz, S E Kopits, et al.
Pageof 6

Showing results (41-50 of 58) with videos related to

Sort By:
Pageof 6
American Journal of Human Genetics|September 1, 1996
Family study and segregation analysis of Tourette syndrome: evidence for a mixed model of inheritanceJ T Walkup, M C LaBuda, H S Singer, et al.
Journal of Medical Genetics|September 9, 2000
Achondroplasia and nail-patella syndrome: the compound phenotypeM J Wright, M C Ain, M V Clough, et al.
The Journal of Pediatrics|May 15, 1998
Sleep-disordered breathing in children with achondroplasiaP J Mogayzel, J L Carroll, G M Loughlin, et al.
Journal of Neurosurgical Anesthesiology|July 25, 2000
Perioperative intracranial hemorrhage in achondroplasia: a case reportI Elmaci, M C Ain, M J Wright, et al.
AJNR. American Journal of Neuroradiology|March 1, 1992
Chromosomal disorders: background and neuroradiologyA J Kumar, T P Naidich, G Stetten, et al.
Neurology|March 1, 1997
Linkage of the locus for cerebral cavernous hemangiomas to human chromosome 7q in four families of Mexican-American descentM H Polymeropoulos, O Hurko, F Hsu, et al.
The Journal of Clinical Investigation|February 1, 1988
Oral carnitine therapy in children with cystinosis and renal Fanconi syndromeW A Gahl, I Bernardini, M Dalakas, et al.
AJNR. American Journal of Neuroradiology|May 1, 1995
Reversibility of white matter changes and dementia after treatment of dural fistulasS M Zeidman, L H Monsein, O Arosarena, et al.
Proceedings of the National Academy of Sciences of the United States of America|May 15, 1992
MELAS mutation in mtDNA binding site for transcription termination factor causes defects in protein synthesis and in respiration but no change in levels of upstream and downstream mature transcriptsA Chomyn, A Martinuzzi, M Yoneda, et al.
Basic Life Sciences|January 1, 1988
Cervicomedullary cord compression in young children with achondroplasia: value of comprehensive neurologic and respiratory evaluationC S Reid, R E Pyeritz, S E Kopits, et al.
Pageof 6