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Human Mutation
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January 8, 2000
New transthyretin variants SER 91 and SER 116 associated with familial amyloidotic polyneuropathy. Mutations in brief no. 151. Online
A M Misrahi, V Plante, T Lalu, et al.
The American Journal of Physiology
|
July 1, 1993
Effect of adenosine on heart rate in isolated muskrat and guinea pig hearts
T A McKean, H Sterling, D R Streeby, et al.
Arthritis and Rheumatism
|
November 1, 1995
Peripheral neuropathy with necrotizing vasculitis in rheumatoid arthritis. A clinicopathologic and prognostic study of thirty-two patients
X Puéchal, G Said, P Hilliquin, et al.
Revue Neurologique
|
January 1, 1992
[Cerebral complications of incontinentia pigmenti. A clinicopathological study of a case]
C Triki, D Devictor, S Kah, et al.
Bone Marrow Transplantation
|
July 16, 2008
Breakthrough Rhizopus infection on posaconazole prophylaxis following allogeneic stem cell transplantation
F Schlemmer, M Lagrange-Xélot, C Lacroix, et al.
Neurology
|
September 25, 1998
Genotypic-phenotypic variations in a series of 65 patients with familial amyloid polyneuropathy
V Planté-Bordeneuve, T Lalu, M Misrahi, et al.
Hypertension (Dallas, Tex. : 1979)
|
October 16, 1999
Plasma homocysteine, aortic stiffness, and renal function in hypertensive patients
L A Bortolotto, M E Safar, E Billaud, et al.
The Journal of Endocrinology
|
May 13, 1999
Ovine chorionic somatomammotrophin (oCS) production by isolated cotyledon cells from sheep in early and mid gestation: auto-regulation by recombinant oCS
M C Soares, J L Servely, C Puissant, et al.
Neurology
|
May 1, 1996
Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts: a new progressive disorder due to diffuse cerebral microangiopathy
P Labrune, C Lacroix, F Goutières, et al.
Annals of Neurology
|
October 12, 2000
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation
V Pingault, A Guiochon-Mantel, N Bondurand, et al.
Page
of 35
Search research articles
Search
Showing results (261-270 of 341) with videos related to
Sort By:
Page
of 35
Human Mutation
|
January 8, 2000
New transthyretin variants SER 91 and SER 116 associated with familial amyloidotic polyneuropathy. Mutations in brief no. 151. Online
A M Misrahi, V Plante, T Lalu, et al.
The American Journal of Physiology
|
July 1, 1993
Effect of adenosine on heart rate in isolated muskrat and guinea pig hearts
T A McKean, H Sterling, D R Streeby, et al.
Arthritis and Rheumatism
|
November 1, 1995
Peripheral neuropathy with necrotizing vasculitis in rheumatoid arthritis. A clinicopathologic and prognostic study of thirty-two patients
X Puéchal, G Said, P Hilliquin, et al.
Revue Neurologique
|
January 1, 1992
[Cerebral complications of incontinentia pigmenti. A clinicopathological study of a case]
C Triki, D Devictor, S Kah, et al.
Bone Marrow Transplantation
|
July 16, 2008
Breakthrough Rhizopus infection on posaconazole prophylaxis following allogeneic stem cell transplantation
F Schlemmer, M Lagrange-Xélot, C Lacroix, et al.
Neurology
|
September 25, 1998
Genotypic-phenotypic variations in a series of 65 patients with familial amyloid polyneuropathy
V Planté-Bordeneuve, T Lalu, M Misrahi, et al.
Hypertension (Dallas, Tex. : 1979)
|
October 16, 1999
Plasma homocysteine, aortic stiffness, and renal function in hypertensive patients
L A Bortolotto, M E Safar, E Billaud, et al.
The Journal of Endocrinology
|
May 13, 1999
Ovine chorionic somatomammotrophin (oCS) production by isolated cotyledon cells from sheep in early and mid gestation: auto-regulation by recombinant oCS
M C Soares, J L Servely, C Puissant, et al.
Neurology
|
May 1, 1996
Extensive brain calcifications, leukodystrophy, and formation of parenchymal cysts: a new progressive disorder due to diffuse cerebral microangiopathy
P Labrune, C Lacroix, F Goutières, et al.
Annals of Neurology
|
October 12, 2000
Peripheral neuropathy with hypomyelination, chronic intestinal pseudo-obstruction and deafness: a developmental "neural crest syndrome" related to a SOX10 mutation
V Pingault, A Guiochon-Mantel, N Bondurand, et al.
Page
of 35