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	41.	Childhood demyelinating diseases with a prolonged remitting course and their relation to Schilder's disease: report of two cases. [electronic resource] by Leuzzi, V Lyon, G Cilio, M R Pedespan, J M Fontan, D Chateil, J F Vital, A Producer: 19990426 In: Journal of neurology, neurosurgery, and psychiatry vol. 66 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	42.	[Botulinum toxin in the management of spastic hip adductors in non-ambulatory cerebral palsy children]. [electronic resource] by Deleplanque, B Lagueny, A Flurin, V Arnaud, C Pedespan, J M Fontan, D Pontallier, J R Producer: 20030521 In: Revue de chirurgie orthopedique et reparatrice de l'appareil moteur vol. 88 Availability: No items available. Save to lists Add to cart (remove)
	43.	[Superior sagittal sinus thrombosis in children during the first year of life: clinical aspects, imaging and development]. [electronic resource] by Pedespan, J M Chateil, J F Pedespan-Joly, L Fontan, D Demarquez, J L Guillard, J M Producer: 19961211 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	44.	[Cerebellar vermis hypoplasia with extracerebral involvement (retina, kidney, liver): difficult to classify syndromes]. [electronic resource] by Graber, D Antignac, C Deschenes, G Coulin, A Hermouet, Y Pedespan, J M Fontan, D Ponsot, G Producer: 20010329 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 8 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	45.	Deletion of 11 amino acids in tuberin associated with severe tuberous sclerosis phenotypes: evidence for a new essential domain in the first third of the protein. [electronic resource] by Jobert, S Bragado-Nilsson, E Samolyk, D Pedespan, J M Marchal, C Reichert, S Mallet, J Pitiot, G Producer: 19980121 In: European journal of human genetics : EJHG vol. 5 Availability: No items available. Save to lists Add to cart (remove)
	46.	[Obstructive hydrocephalus and Crouzon syndrome]. [electronic resource] by Levesque, D Coste, V Gimbert, E Duval, M-V Pedespan, J-M Lafourcade, J-P Korobelnik, J-F Producer: 20191028 In: Journal francais d'ophtalmologie vol. 42 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	47.	[Temporal lobe epilepsy and ganglioglioma in children. Clinical aspects, imagery and neuropathology; nosological discussion of six cases]. [electronic resource] by Brissaud, O Pedespan, J M Chateil, J F Loiseau, H Dautheribes, M Wardi, Y Brun, M Rougier, A Producer: 19981120 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 5 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	48.	[Cutaneous manifestations of Kawasaki disease. Apropos of 30 cases]. [electronic resource] by Ducos, M H Taïeb, A Sarlangue, J Perel, Y Pedespan, J M Hehunstre, J P Jimenez, M Maleville, J Producer: 19940517 In: Annales de dermatologie et de venereologie vol. 120 Availability: No items available. Save to lists Add to cart (remove)
	49.	[Polymorphic expression of epilepsy and cognitive impairment in ring chromosome 20 syndrome]. [electronic resource] by Villéga, F Ngayap, H Espil-Taris, C Husson, M Rooryck-Thambo, C Arveiler, B Lacombe, D Pédespan, J-M Producer: 20110803 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 18 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	50.	[Angelman syndrome and intracranial aneurysm: fortuitous association or commune genetic predisposition?]. [electronic resource] by Meyer Witte, S Espil-Taris, C Cenraud, C Le Brun, S Loiseau, H Chateil, J F Lacombe, D Pédespan, J M Producer: 20060127 In: Archives de pediatrie : organe officiel de la Societe francaise de pediatrie vol. 12 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	51.	Cranial aneurysmal bone cysts presenting with raised intracranial pressure: report of two cases. [electronic resource] by Chateil, J F Dousset, V Meyer, P Pedespan, J M San-Galli, F Rivel, J Caillé, J M Diard, F Producer: 19971010 In: Neuroradiology vol. 39 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	52.	Interferon-beta treatment in patients with childhood-onset multiple sclerosis. [electronic resource] by Mikaeloff, Y Moreau, T Debouverie, M Pelletier, J Lebrun, C Gout, O Pedespan, J M Van Hulle, C Vermersch, P Ponsot, G Producer: 20011018 In: The Journal of pediatrics vol. 139 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	53.	Menkes disease: study of the mitochondrial respiratory chain in three cases. [electronic resource] by Pedespan, J M Jouaville, L S Cances, C Letellier, T Malgat, M Guiraud, P Coquet, M Vernhet, I Lacombe, D Mazat, J P Producer: 19991004 In: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society vol. 3 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	54.	X-linked myopathy with excessive autophagy: a clinicopathological study of five new families. [electronic resource] by Chabrol, B Figarella-Branger, D Coquet, M Mancini, J Fontan, D Pedespan, J M Francannet, C Pouget, J Beaufrère, A M Pellissier, J F Producer: 20010719 In: Neuromuscular disorders : NMD vol. 11 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	55.	Statistical analysis of mitochondrial pathologies in childhood: identification of deficiencies using principal component analysis. [electronic resource] by Letellier, T Durrieu, G Malgat, M Rossignol, R Antoch, J Deshouillers, J M Coquet, M Lacombe, D Netter, J C Pedespan, J M Redonnet-Vernhet, I Mazat, J P Producer: 20000801 In: Laboratory investigation; a journal of technical methods and pathology vol. 80 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	56.	Infantile Alexander disease: spectrum of GFAP mutations and genotype-phenotype correlation. [electronic resource] by Rodriguez, D Gauthier, F Bertini, E Bugiani, M Brenner, M N'guyen, S Goizet, C Gelot, A Surtees, R Pedespan, J M Hernandorena, X Troncoso, M Uziel, G Messing, A Ponsot, G Pham-Dinh, D Dautigny, A Boespflug-Tanguy, O Producer: 20011207 In: American journal of human genetics vol. 69 Online resources: Available from publisher's website Availability: No items available. Save to lists Add to cart (remove)
	57.	Collaborative study of mosaic tetrasomy 12p or Pallister-Killian syndrome (nineteen fetuses or children). [electronic resource] by Mathieu, M Piussan, C Thepot, F Gouget, A Lacombe, D Pedespan, J M Serville, F Fontan, D Ruffie, M Nivelon-Chevallier, A Amblard, F Chauveau, P Moirot, H Chabrolle, J P Croquette, M F Teyssier, M Plauchu, H Pelissier, M C Gilgenkrantz, S Turc-Carel, C Turleau, C Prieur, M Le Merrer, M Gonzales, M Journel, H Producer: 19970610 In: Annales de genetique vol. 40 Availability: No items available. Save to lists Add to cart (remove)