Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

Search Results

2,307 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Results By Year timeline is not available.
Page 1
[Fetal neurology: conditions of diagnostic uncertainty].
Moutard ML, Gélot A, Rodriguez D, Guët A, Mignot C, Ponsot G, Billette de Villemeur T. Moutard ML, et al. Among authors: rodriguez d. Arch Pediatr. 2006 Jun;13(6):825-7. doi: 10.1016/j.arcped.2006.03.128. Epub 2006 May 12. Arch Pediatr. 2006. PMID: 16698255 French. No abstract available.
[Role of neuropediatrics in prenatal diagnosis].
Moutard ML, Lewin F, Adamsbaum C, Gélot A, Rodriguez D, Ponsot G. Moutard ML, et al. Among authors: rodriguez d. Arch Pediatr. 2001 May;8 Suppl 2:442s-444s. doi: 10.1016/s0929-693x(01)80103-2. Arch Pediatr. 2001. PMID: 11394145 French. No abstract available.
Progressive megalencephaly due to specific EIF2Bepsilon mutations in two unrelated families.
Passemard S, Gelot A, Fogli A, N'Guyen S, Barnerias C, Niel F, Doummar D, Arbues AS, Mignot C, de Villemeur TB, Ponsot G, Boespflug-Tanguy O, Rodriguez D. Passemard S, et al. Among authors: rodriguez d. Neurology. 2007 Jul 24;69(4):400-2. doi: 10.1212/01.wnl.0000266388.02772.f8. Neurology. 2007. PMID: 17646634 No abstract available.
[Severe anorexia in infants in Reunion: a new autosomal recessive disease?].
Renouil M, Fourmaintraux A, Cartault F, Rodriguez D, Razafinarivo-Schoreitz S, Chaurand G, Wendling C, Bangui A, Ponsot G. Renouil M, et al. Among authors: rodriguez d. Arch Pediatr. 1999 Jul;6(7):725-34. doi: 10.1016/s0929-693x(99)80354-6. Arch Pediatr. 1999. PMID: 10429812 French.
Using medical exome sequencing to identify the causes of neurodevelopmental disorders: Experience of 2 clinical units and 216 patients.
Chérot E, Keren B, Dubourg C, Carré W, Fradin M, Lavillaureix A, Afenjar A, Burglen L, Whalen S, Charles P, Marey I, Heide S, Jacquette A, Heron D, Doummar D, Rodriguez D, Billette de Villemeur T, Moutard ML, Guët A, Xavier J, Périsse D, Cohen D, Demurger F, Quélin C, Depienne C, Odent S, Nava C, David V, Pasquier L, Mignot C. Chérot E, et al. Among authors: rodriguez d. Clin Genet. 2018 Mar;93(3):567-576. doi: 10.1111/cge.13102. Epub 2017 Oct 4. Clin Genet. 2018. PMID: 28708303 Free article.
Pontoneocerebellar hypoplasia: definition of MR features.
Goasdoué P, Rodriguez D, Moutard ML, Robain O, Lalande G, Adamsbaum C. Goasdoué P, et al. Among authors: rodriguez d. Pediatr Radiol. 2001 Sep;31(9):613-8. doi: 10.1007/s002470100507. Pediatr Radiol. 2001. PMID: 11511999
2,307 results