Showing results (51-60 of 177) with videos related to

Sort By:
Pageof 18
Neuromuscular Disorders : NMD|June 9, 2009
Novel mutations in the GDAP1 gene in patients affected with early-onset axonal Charcot-Marie-Tooth type 4AIsabella Moroni, Michela Morbin, Micaela Milani, et al.
Evolutionary Biology|December 11, 2012
Evo-Devo of the Human Vertebral Column: On Homeotic Transformations, Pathologies and Prenatal SelectionClara M A Ten Broek, Alexander J Bakker, Irma Varela-Lasheras, et al.
Scientific Reports|January 16, 2014
Higher limb asymmetry in deceased human fetuses and infants with aneuploidyJessica Bots, Clara M A ten Broek, Jeroen A M Belien, et al.
Nederlands Tijdschrift Voor Geneeskunde|September 24, 2023
[Adhesive small bowel obstruction after surgery during infancy; a potentially fatal long term complication]Fenne A I M van den Bunder, Dirk-Jan van Zuidam, Esther Edelenbos, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|June 7, 2006
Rhythmic cortical myoclonus in Niemann-Pick disease type CLaura Canafoglia, Marianna Bugiani, Graziella Uziel, et al.
Neuropediatrics|November 28, 2017
4H Leukodystrophy: Lessons from 3T ImagingFerdy K Cayami, Marianna Bugiani, Petra J W Pouwels, et al.
Acta Neuropathologica|August 10, 2025
A focus on the normal-appearing white and gray matter within the multiple sclerosis brain: a link to smoldering progressionGema Muñoz González, Bert A T Hart, Marianna Bugiani, et al.
Neurocase|December 26, 2018
Neuro-Behçet's disease presenting as an isolated progressive cognitive and behavioral syndromeDario Saracino, Lia Allegorico, Anna Maria Barbarulo, et al.
Annals of Neurology|September 5, 2002
X-linked creatine deficiency syndrome: a novel mutation in creatine transporter gene SLC6A8Alberto Bizzi, Marianna Bugiani, Gajja S Salomons, et al.
Neuropediatrics|December 1, 2015
Absent Thalami Caused by a Homozygous EARS2 Mutation: Expanding Disease Spectrum of LTBLSietske H Kevelam, Femke C C Klouwer, Johanna M Fock, et al.
Pageof 18