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Human Molecular Genetics
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December 1, 1996
Frameshift mutation in the survival motor neuron gene in a severe case of SMA type I
C Brahe, O Clermont, S Zappata, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
April 1, 1997
The cardio-facio-cutaneous syndrome: a long-term follow-up of two patients, with special reference to the neurological features
G Sabatino, A Verrotti, S Domizio, et al.
Histology and Histopathology
|
May 16, 2000
Prolonged kallikrein inhibition does not affect the basal growth and secretory capacity of rat adrenal cortex, but enhances mineralo- and glucocorticoid response to ACTH and handling stress
P Rebuffat, G Neri, M Bahçelioglu, et al.
Journal of Immunological Methods
|
January 29, 2000
Infrared photodetection for the in vivo localisation of phage-derived antibodies directed against angiogenic markers
M Birchler, G Neri, L Tarli, et al.
International Journal of Molecular Medicine
|
December 15, 2000
Buffering action of endogenous nitric oxide on the adrenocortical secretagogue effect of endothelins in the rat
G Mazzocchi, G Neri, L K Malendowicz, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri
|
October 1, 1983
[Organization of nocturnal sleep in 41 hospitalized patients: evaluation of the first night effect]
G Mennuni, M Morante, L Strusi, et al.
Bollettino Chimico Farmaceutico
|
February 1, 1989
Particulate matter in small volume parenterals: evaluation of some technological and analytical aspects
E Cirannni Signoretti, I Montanari, G Neri, et al.
American Journal of Medical Genetics
|
September 1, 1984
The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies
G Neri, M E Martini-Neri, B E Katz, et al.
American Journal of Medical Genetics
|
February 1, 1983
A boy with ring chromosome 15 derived from a t(15q;15q) Robertsonian translocation in the mother: cytogenetic and biochemical findings
G Neri, R Ricci, A Pelino, et al.
American Journal of Medical Genetics
|
June 1, 1989
A case of the Freire-Maia Odontotrichomelic syndrome: nosology with EEC syndrome
L Pavone, R Rizzo, A Tiné, et al.
Page
of 63
Search research articles
Search
Showing results (251-260 of 628) with videos related to
Sort By:
Page
of 63
Human Molecular Genetics
|
December 1, 1996
Frameshift mutation in the survival motor neuron gene in a severe case of SMA type I
C Brahe, O Clermont, S Zappata, et al.
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
April 1, 1997
The cardio-facio-cutaneous syndrome: a long-term follow-up of two patients, with special reference to the neurological features
G Sabatino, A Verrotti, S Domizio, et al.
Histology and Histopathology
|
May 16, 2000
Prolonged kallikrein inhibition does not affect the basal growth and secretory capacity of rat adrenal cortex, but enhances mineralo- and glucocorticoid response to ACTH and handling stress
P Rebuffat, G Neri, M Bahçelioglu, et al.
Journal of Immunological Methods
|
January 29, 2000
Infrared photodetection for the in vivo localisation of phage-derived antibodies directed against angiogenic markers
M Birchler, G Neri, L Tarli, et al.
International Journal of Molecular Medicine
|
December 15, 2000
Buffering action of endogenous nitric oxide on the adrenocortical secretagogue effect of endothelins in the rat
G Mazzocchi, G Neri, L K Malendowicz, et al.
Rivista Di Neurobiologia : Organo Ufficiale Della Societa Dei Neurologi, Neuroradiologi E Neurochirurghi Ospedalieri
|
October 1, 1983
[Organization of nocturnal sleep in 41 hospitalized patients: evaluation of the first night effect]
G Mennuni, M Morante, L Strusi, et al.
Bollettino Chimico Farmaceutico
|
February 1, 1989
Particulate matter in small volume parenterals: evaluation of some technological and analytical aspects
E Cirannni Signoretti, I Montanari, G Neri, et al.
American Journal of Medical Genetics
|
September 1, 1984
The Perlman syndrome: familial renal dysplasia with Wilms tumor, fetal gigantism and multiple congenital anomalies
G Neri, M E Martini-Neri, B E Katz, et al.
American Journal of Medical Genetics
|
February 1, 1983
A boy with ring chromosome 15 derived from a t(15q;15q) Robertsonian translocation in the mother: cytogenetic and biochemical findings
G Neri, R Ricci, A Pelino, et al.
American Journal of Medical Genetics
|
June 1, 1989
A case of the Freire-Maia Odontotrichomelic syndrome: nosology with EEC syndrome
L Pavone, R Rizzo, A Tiné, et al.
Page
of 63