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L Haataja

Showing results (21-30 of 44) with videos related to

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Genomics|May 20, 1995
Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15J Schleutker, A P Laine, L Haataja, et al.
Cancer Research|May 15, 1994
Cellular interactions of CRKL, and SH2-SH3 adaptor proteinJ ten Hoeve, V Kaartinen, T Fioretos, et al.
Neuropediatrics|August 30, 2002
MRI lesions and infants with neonatal encephalopathy. Is the Apgar score predictive?E Mercuri, M Rutherford, A Barnett, et al.
Archives of Disease in Childhood|June 24, 2004
Can the Griffiths scales predict neuromotor and perceptual-motor impairment in term infants with neonatal encephalopathy?A L Barnett, A Guzzetta, E Mercuri, et al.
Neuropediatrics|January 22, 2003
Neurological and perceptual-motor outcome at 5 - 6 years of age in children with neonatal encephalopathy: relationship with neonatal brain MRIA Barnett, E Mercuri, M Rutherford, et al.
American Journal of Human Genetics|July 1, 1993
Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)J Körkkö, P Ritvaniemi, L Haataja, et al.
Molecular and Cellular Biology|March 1, 1996
Inhibition of Bcr serine kinase by tyrosine phosphorylationJ Liu, Y Wu, G Z Ma, et al.
Neuropediatrics|July 13, 1999
Neonatal neurological examination in infants with hypoxic ischaemic encephalopathy: correlation with MRI findingsE Mercuri, A Guzzetta, L Haataja, et al.
Annals of Tropical Paediatrics|February 24, 2001
Neonatal neurological testing in resource-poor settingsR McGready, J Simpson, S Panyavudhikrai, et al.
Development (Cambridge, England)|October 31, 2001
Abnormal function of astroglia lacking Abr and Bcr RacGAPsV Kaartinen, I Gonzalez-Gomez, J W Voncken, et al.
Pageof 5

Showing results (21-30 of 44) with videos related to

Sort By:
Pageof 5
Genomics|May 20, 1995
Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15J Schleutker, A P Laine, L Haataja, et al.
Cancer Research|May 15, 1994
Cellular interactions of CRKL, and SH2-SH3 adaptor proteinJ ten Hoeve, V Kaartinen, T Fioretos, et al.
Neuropediatrics|August 30, 2002
MRI lesions and infants with neonatal encephalopathy. Is the Apgar score predictive?E Mercuri, M Rutherford, A Barnett, et al.
Archives of Disease in Childhood|June 24, 2004
Can the Griffiths scales predict neuromotor and perceptual-motor impairment in term infants with neonatal encephalopathy?A L Barnett, A Guzzetta, E Mercuri, et al.
Neuropediatrics|January 22, 2003
Neurological and perceptual-motor outcome at 5 - 6 years of age in children with neonatal encephalopathy: relationship with neonatal brain MRIA Barnett, E Mercuri, M Rutherford, et al.
American Journal of Human Genetics|July 1, 1993
Mutation in type II procollagen (COL2A1) that substitutes aspartate for glycine alpha 1-67 and that causes cataracts and retinal detachment: evidence for molecular heterogeneity in the Wagner syndrome and the Stickler syndrome (arthro-ophthalmopathy)J Körkkö, P Ritvaniemi, L Haataja, et al.
Molecular and Cellular Biology|March 1, 1996
Inhibition of Bcr serine kinase by tyrosine phosphorylationJ Liu, Y Wu, G Z Ma, et al.
Neuropediatrics|July 13, 1999
Neonatal neurological examination in infants with hypoxic ischaemic encephalopathy: correlation with MRI findingsE Mercuri, A Guzzetta, L Haataja, et al.
Annals of Tropical Paediatrics|February 24, 2001
Neonatal neurological testing in resource-poor settingsR McGready, J Simpson, S Panyavudhikrai, et al.
Development (Cambridge, England)|October 31, 2001
Abnormal function of astroglia lacking Abr and Bcr RacGAPsV Kaartinen, I Gonzalez-Gomez, J W Voncken, et al.
Pageof 5