Profil bibliographique

M. Tauber

Informations fournies par OpenAlex. Research Africa ne déduit ni nationalité, ni poste, ni coordonnées personnelles.

341Publications signalées

9729Citations signalées

9Affiliations récentes

Institutions déclarées

Centre National de la Recherche Scientifique Université Toulouse III - Paul Sabatier Inserm Université Fédérale de Toulouse Midi-Pyrénées Advisory Board Company (United States)Centre Hospitalier Universitaire de Toulouse Toulouse Mathematics Institute Hôpital des Enfants Institut Toulousain des Maladies Infectieuses et Inflammatoires

Domaines associés

Genetic Syndromes and ImprintingGrowth Hormone and Insulin-like Growth FactorsGenetics and Neurodevelopmental DisordersSexual Differentiation and DisordersEpigenetics and DNA Methylation

Publications récentes

Accès ouvert 2026 articleOpenAlex

Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsJournal of Neurodevelopmental Disorders

Accès ouvert 2026 articleOpenAlex

Additional file 2 of Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 articleOpenAlex

Additional file 3 of Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 otherOpenAlex

Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 articleOpenAlex

Additional file 1 of Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 articleOpenAlex

Additional file 3 of Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 otherOpenAlex

Additional file 4 of Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 articleOpenAlex

Additional file 1 of Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 otherOpenAlex

Additional file 4 of Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 articleOpenAlex

Additional file 2 of Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

Accès ouvert 2026 otherOpenAlex

Early neurodevelopmental brain perfusion abnormalities and functional connectivity findings in infants with Prader-Willi syndrome

Jennifer Boisgontier, Sarah Charpy, Graziella Pinto, Volodia Dangouloff-Ros et autres

0 citationsFigshare

2026 articleOpenAlex

Circulating levels of ghrelin and hyperphagia in patients with rare genetic neurodevelopmental disorders

Gwénaëlle Diene, Grégoire Benvegnu, Cathy Brochado, Alice Clerc et autres

1 citationThe Journal of Clinical Endocrinology & Metabolism

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