Samuel Rotman
AuthID: R-007-314
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TITLE: Two new families with hereditary minimal change disease Full Text
AUTHORS: Hassib Chehade; Francois Cachat; Eric Girardin; Samuel Rotman; Antonio Jorge Correia; Florence Fellmann; Olivier Bonny;
PUBLISHED: 2013, SOURCE: BMC NEPHROLOGY, VOLUME: 14, ISSUE: 1
AUTHORS: Hassib Chehade; Francois Cachat; Eric Girardin; Samuel Rotman; Antonio Jorge Correia; Florence Fellmann; Olivier Bonny;
PUBLISHED: 2013, SOURCE: BMC NEPHROLOGY, VOLUME: 14, ISSUE: 1
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TITLE: Deletion of the neuropeptide Y (NPY) Y-1 receptor gene reveals a regulatory role of NPY on catecholamine synthesis and secretion
AUTHORS: Claudia Cavadas ; Daniel Cefai; Joana Rosmaninho Salgado ; Maria Augusta Vieira Coelho ; Eduardo Moura; Nathalie Busso; Thierry Pedrazzini; Daniela Grand; Samuel Rotman; Bernard Waeber; Jean Francois Aubert; Eric Grouzmann;
PUBLISHED: 2006, SOURCE: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, VOLUME: 103, ISSUE: 27
AUTHORS: Claudia Cavadas ; Daniel Cefai; Joana Rosmaninho Salgado ; Maria Augusta Vieira Coelho ; Eduardo Moura; Nathalie Busso; Thierry Pedrazzini; Daniela Grand; Samuel Rotman; Bernard Waeber; Jean Francois Aubert; Eric Grouzmann;
PUBLISHED: 2006, SOURCE: PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, VOLUME: 103, ISSUE: 27
