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Radiology
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June 1, 1990
Spondylometaphyseal dysplasia, corner fracture type: a heritable condition associated with coxa vara
L O Langer, P W Brill, M B Ozonoff, et al.
The American Journal of Roentgenology, Radium Therapy, and Nuclear Medicine
|
April 1, 1975
The Kniest syndrome
R S Lachman, D L Rimoin, D W Hollister, et al.
American Journal of Medical Genetics. Part A
|
August 25, 2004
Spondylometaphyseal dysplasia with cone-rod dystrophy
Brent A Walters, Michael L Raff, James Ver Hoeve, et al.
Bioorganic & Medicinal Chemistry
|
April 20, 2001
Synthesis of high-specific-radioactivity 4- and 6-[18F]fluorometaraminol-PET tracers for the adrenergic nervous system of the heart
O Langer, F Dollé, H Valette, et al.
American Journal of Medical Genetics
|
October 1, 1984
Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology
C B Whitley, L O Langer, J Ophoven, et al.
Current Alzheimer Research
|
June 13, 2009
Amyloid PET and MRI in Alzheimer's disease and mild cognitive impairment
E Dimou, J Booij, M Rodrigues, et al.
American Journal of Medical Genetics
|
January 1, 1983
A new short rib syndrome: report of two cases
F A Beemer, L O Langer, J M Klep-de Pater, et al.
The Journal of Pediatrics
|
October 1, 1986
A new skeletal dysplasia: clinical, radiologic, and pathologic findings
B K Burton, T Sumner, L O Langer, et al.
American Journal of Medical Genetics
|
February 15, 1993
Further delineation of spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type, with emphasis on diagnostic features
L O Langer, B J Wolfson, C I Scott, et al.
British Journal of Cancer
|
May 14, 2009
FDG uptake is a surrogate marker for defining the optimal biological dose of the mTOR inhibitor everolimus in vivo
D Cejka, C Kuntner, M Preusser, et al.
Page
of 20
Search research articles
Search
Showing results (181-190 of 197) with videos related to
Sort By:
Page
of 20
Radiology
|
June 1, 1990
Spondylometaphyseal dysplasia, corner fracture type: a heritable condition associated with coxa vara
L O Langer, P W Brill, M B Ozonoff, et al.
The American Journal of Roentgenology, Radium Therapy, and Nuclear Medicine
|
April 1, 1975
The Kniest syndrome
R S Lachman, D L Rimoin, D W Hollister, et al.
American Journal of Medical Genetics. Part A
|
August 25, 2004
Spondylometaphyseal dysplasia with cone-rod dystrophy
Brent A Walters, Michael L Raff, James Ver Hoeve, et al.
Bioorganic & Medicinal Chemistry
|
April 20, 2001
Synthesis of high-specific-radioactivity 4- and 6-[18F]fluorometaraminol-PET tracers for the adrenergic nervous system of the heart
O Langer, F Dollé, H Valette, et al.
American Journal of Medical Genetics
|
October 1, 1984
Fibrochondrogenesis: lethal, autosomal recessive chondrodysplasia with distinctive cartilage histopathology
C B Whitley, L O Langer, J Ophoven, et al.
Current Alzheimer Research
|
June 13, 2009
Amyloid PET and MRI in Alzheimer's disease and mild cognitive impairment
E Dimou, J Booij, M Rodrigues, et al.
American Journal of Medical Genetics
|
January 1, 1983
A new short rib syndrome: report of two cases
F A Beemer, L O Langer, J M Klep-de Pater, et al.
The Journal of Pediatrics
|
October 1, 1986
A new skeletal dysplasia: clinical, radiologic, and pathologic findings
B K Burton, T Sumner, L O Langer, et al.
American Journal of Medical Genetics
|
February 15, 1993
Further delineation of spondylo-meta-epiphyseal dysplasia, short limb-abnormal calcification type, with emphasis on diagnostic features
L O Langer, B J Wolfson, C I Scott, et al.
British Journal of Cancer
|
May 14, 2009
FDG uptake is a surrogate marker for defining the optimal biological dose of the mTOR inhibitor everolimus in vivo
D Cejka, C Kuntner, M Preusser, et al.
Page
of 20