Chateil JF - Search Results

1

Confirmation of Atypical Presentation With Nonprogressive Leukodystrophy in eIF2B-Related Disorders.

Scappaticci C, Van-Gils J, Samaan S, Bessou P, Lacombe D, Chateil JF, Pedespan JM, Saves JL, Boespflug-Tanguy O, Goizet C. Scappaticci C, et al. Among authors: chateil jf. Pediatr Neurol. 2019 Nov;100:97-99. doi: 10.1016/j.pediatrneurol.2019.02.005. Epub 2019 Mar 1. Pediatr Neurol. 2019. PMID: 31262560 No abstract available.

2

Magnetic resonance imaging diagnosis of subependymal giant cell astrocytomas in follow-up of children with tuberous sclerosis complex: should we always use contrast enhancement?

Gaillard AL, Crombé A, Jecko V, Bessou P, Havez M, Pédespan JM, Van Gils J, Chateil JF. Gaillard AL, et al. Among authors: chateil jf. Pediatr Radiol. 2020 Sep;50(10):1397-1408. doi: 10.1007/s00247-020-04707-z. Epub 2020 Jul 15. Pediatr Radiol. 2020. PMID: 32671416

3

Hemidystonia with polymicrogyria is part of ATP1A3-related disorders.

Lacombe D, Van-Gils J, Lebrun M, Trimouille A, Michaud V, Cabet S, Chateil JF, Pedespan JM, Bar C, Lesca G. Lacombe D, et al. Among authors: chateil jf. Brain Dev. 2022 Sep;44(8):567-570. doi: 10.1016/j.braindev.2022.05.001. Epub 2022 May 24. Brain Dev. 2022. PMID: 35623960

4

Refractory occipital lobe epilepsy treated by surgery in a child with chronic encephalitis.

Rougier A, Vital A, Michel V, Chateil JF, Husson M, Pedespan JM. Rougier A, et al. Among authors: chateil jf. Pediatr Neurosurg. 2007;43(2):130-3. doi: 10.1159/000098387. Pediatr Neurosurg. 2007. PMID: 17337926

5

A patient with hydranencephaly and PEHO-like dysmorphic features.

Goizet C, Espil-Taris C, Husson M, Chateil JF, Pedespan JM, Lacombe D. Goizet C, et al. Among authors: chateil jf. Ann Genet. 2003 Jan-Mar;46(1):25-8. doi: 10.1016/s0003-3995(03)00003-0. Ann Genet. 2003. PMID: 12818526

6

SMAD4 germinal mosaicism in a family with juvenile polyposis and hypertrophic osteoarthropathy.

Lamireau T, Olschwang S, Rooryck C, Le Bail B, Chateil JF, Lacombe D. Lamireau T, et al. Among authors: chateil jf. J Pediatr Gastroenterol Nutr. 2005 Jul;41(1):117-20. doi: 10.1097/01.mpg.0000151762.51287.7d. J Pediatr Gastroenterol Nutr. 2005. PMID: 15990641 No abstract available.

7

Neurofibromatosis type 1 with undescribed osseous abnormalities: new features?

Leruste A, Chateil JF, Ramirez S, Bellanné C, Vidaud D, Lacombe D. Leruste A, et al. Among authors: chateil jf. Clin Dysmorphol. 2009 Apr;18(2):92-94. doi: 10.1097/MCD.0b013e3283279a28. Clin Dysmorphol. 2009. PMID: 19238080 No abstract available.

8

Intracranial empyema complicating sinusitis in childhood: Epidemiology, imaging findings and outcome.

Agouzoul S, Coelho J, Sagardoy T, Delmas J, Bessou P, Havez M, Ollivier M, Chateil JF. Agouzoul S, et al. Among authors: chateil jf. Int J Pediatr Otorhinolaryngol. 2022 Nov;162:111299. doi: 10.1016/j.ijporl.2022.111299. Epub 2022 Sep 5. Int J Pediatr Otorhinolaryngol. 2022. PMID: 36137474

9

Costello syndrome and neurological abnormalities.

Delrue MA, Chateil JF, Arveiler B, Lacombe D. Delrue MA, et al. Among authors: chateil jf. Am J Med Genet A. 2003 Dec 15;123A(3):301-5. doi: 10.1002/ajmg.a.20330. Am J Med Genet A. 2003. PMID: 14608654 Review.

10

Association of external auditory canal atresia, vertical talus, and hypertelorism: confirmation of Rasmussen syndrome.

Julia S, Pedespan JM, Boudard P, Barbier R, Gavilan-Cellie I, Chateil JF, Lacombe D. Julia S, et al. Among authors: chateil jf. Am J Med Genet. 2002 Jun 15;110(2):179-81. doi: 10.1002/ajmg.10433. Am J Med Genet. 2002. PMID: 12116258

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