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Genomics
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May 20, 1995
Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15
J Schleutker, A P Laine, L Haataja, et al.
Cancer Research
|
May 15, 1994
Cellular interactions of CRKL, and SH2-SH3 adaptor protein
J 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 MRI
A 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 phosphorylation
J Liu, Y Wu, G Z Ma, et al.
Neuropediatrics
|
July 13, 1999
Neonatal neurological examination in infants with hypoxic ischaemic encephalopathy: correlation with MRI findings
E Mercuri, A Guzzetta, L Haataja, et al.
Annals of Tropical Paediatrics
|
February 24, 2001
Neonatal neurological testing in resource-poor settings
R McGready, J Simpson, S Panyavudhikrai, et al.
Development (Cambridge, England)
|
October 31, 2001
Abnormal function of astroglia lacking Abr and Bcr RacGAPs
V Kaartinen, I Gonzalez-Gomez, J W Voncken, et al.
Page
of 5
Search research articles
Search
Showing results (21-30 of 44) with videos related to
Sort By:
Page
of 5
Genomics
|
May 20, 1995
Linkage disequilibrium utilized to establish a refined genetic position of the Salla disease locus on 6q14-q15
J Schleutker, A P Laine, L Haataja, et al.
Cancer Research
|
May 15, 1994
Cellular interactions of CRKL, and SH2-SH3 adaptor protein
J 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 MRI
A 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 phosphorylation
J Liu, Y Wu, G Z Ma, et al.
Neuropediatrics
|
July 13, 1999
Neonatal neurological examination in infants with hypoxic ischaemic encephalopathy: correlation with MRI findings
E Mercuri, A Guzzetta, L Haataja, et al.
Annals of Tropical Paediatrics
|
February 24, 2001
Neonatal neurological testing in resource-poor settings
R McGready, J Simpson, S Panyavudhikrai, et al.
Development (Cambridge, England)
|
October 31, 2001
Abnormal function of astroglia lacking Abr and Bcr RacGAPs
V Kaartinen, I Gonzalez-Gomez, J W Voncken, et al.
Page
of 5