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Journal De Radiologie|August 1, 1985
[Value of ultrasonography in the diagnosis of cirrhoses. Prospective study of 128 patients]P Richard, P Bonniaud, C Barthélémy, et al.Journal of Neurology, Neurosurgery, and Psychiatry|November 18, 2009
Clinical and mutational spectrum of limb-girdle muscular dystrophy type 2I in 11 French patientsH Bourteel, P Vermersch, J-M Cuisset, et al.Advances in Experimental Medicine and Biology|February 23, 1999
New aspects of firing pattern autocontrol in oxytocin and vasopressin neuronesF Moos, L Gouzènes, D Brown, et al.Fundamental & Clinical Pharmacology|January 1, 1993
Pharmacokinetics of apomorphine in parkinsonian patientsE Nicolle, P Pollak, F Serre-Debeauvais, et al.Nucleic Acids Research|November 21, 2007
Ex vivo correction of selenoprotein N deficiency in rigid spine muscular dystrophy caused by a mutation in the selenocysteine codonM Rederstorff, V Allamand, P Guicheney, et al.Journal of Neuroendocrinology|February 14, 2009
Oxytocin in the bed nucleus of the stria terminalis and lateral septum facilitates bursting of hypothalamic oxytocin neurons in suckled ratsF Moos, C D Ingram, J B Wakerley, et al.Revue Neurologique|March 14, 2007
[Phenotypic aspects of FKRP-linked muscular dystrophy type 2I in a series of eleven patients]H Bourteel, T Stojkovic, J M Cuisset, et al.The Journal of Physical Chemistry. A|June 16, 2007
Enhancement of a Lewis acid-base interaction via solvation: ammonia molecules and the benzene radical cationChi-Tung Chiang, Marek Freindorf, Thomas Furlani, et al.Clinical Science (London, England : 1979)|July 1, 1997
Compound heterozygote for both rare apolipoprotein E1 (Gly127-->Asp, Arg158-->Cys) and E3(Cys112-->Arg, Arg251-->Gly) alleles in a multigeneration pedigree with hyperlipoproteinaemiaP Richard, I Beucler, M Pascual De Zulueta, et al.Communications Biology|November 6, 2023
The DNA-binding induced (de)AMPylation activity of a Coxiella burnetii Fic enzyme targets Histone H3Dorothea Höpfner, Adam Cichy, Vivian Pogenberg, et al.Pageof 120