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Carneiro, Maryline
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1

Vision du pédiatre:

Rougeot-jung, Christelle ; Poulat, Anne Lise ; Decrette, Emilie...
Revue Neurologique.  180 (2024)  - p. S183 , 2024
Link: https://doi.org/10.1016/..
 
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2

Thrombose veineuse cérébrale de l'enfant:

Carneiro, Maryline
Revue Neurologique.  179 (2023)  - p. S195-S196 , 2023
Link: https://doi.org/10.1016/..
 
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3

New insights into the clinical and molecular spectrum of th..:

Begemann, Anaïs ; Sticht, Heinrich ; Begtrup, Amber...
Genetics in Medicine.  23 (2021)  3 - p. 543-554 , 2021
Link: https://doi.org/10.1038/..
 
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4

Reading Comprehension Impairment in Children With Neurofibr..:

Biotteau, Maëlle ; Tournay, Elodie ; Baudou, Eloise...
Journal of Child Neurology.  36 (2021)  8 - p. 625-634 , 2021
Link: https://doi.org/10.1177/..
 
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5

Description of a novel patient with the TRPM3 recurrent p.V..:

Gauthier, Lucas W ; Chatron, Nicolas ; Cabet, Sara...
European Journal of Medical Genetics.  64 (2021)  11 - p. 104320 , 2021
Link: https://doi.org/10.1016/..
 
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6

Defining the phenotype ofFHF1developmental and epileptic en..:

Trivisano, Marina ; Ferretti, Alessandro ; Bebin, Elizabeth...
Epilepsia.  61 (2020)  7 - p. , 2020
Link: https://doi.org/10.1111/..
 
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7

A novel truncating variant p.(Arg297*) in the GRM1 gene cau..:

Cabet, Sara ; Putoux, Audrey ; Carneiro, Maryline...
European Journal of Medical Genetics.  62 (2019)  10 - p. 103726 , 2019
Link: https://doi.org/10.1016/..
 
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8

Spatially clustering de novo variants in CYFIP2, encoding t..:

Deciphering Developmental Disorders (DDD) Study ; Zweier, Markus ; Begemann, Anaïs...
European Journal of Human Genetics.  27 (2019)  5 - p. 747-759 , 2019
Link: https://doi.org/10.1038/..
 
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9

Postnatal clinical phenotype of five patients with Palliste..:

Alqahtani, Amerh Salem ; Putoux, Audrey ; Bonnet Dupeyron, Marie Noelle...
Molecular Genetics & Genomic Medicine.  7 (2019)  10 - p. , 2019
Link: https://doi.org/10.1002/..
 
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10

Novel homozygous missense variant of GRIN1 in two sibs with..:

Rossi, Massimiliano ; Chatron, Nicolas ; Labalme, Audrey...
European Journal of Human Genetics.  25 (2017)  3 - p. 376-380 , 2017
Link: https://doi.org/10.1038/..
 
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11

MOG antibody-related disorders: common features and uncommo..:

Cobo-Calvo, Álvaro ; Ruiz, Anne ; D'Indy, Hyacintha...
Journal of Neurology.  264 (2017)  9 - p. 1945-1955 , 2017
Link: https://doi.org/10.1007/..
 
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12

Systematic MRI in NF1 children under six years of age for t..:

Blanchard, Gaelle ; Lafforgue, Marie-Pierre ; Lion-François, Laurence...
European Journal of Paediatric Neurology.  20 (2016)  2 - p. 275-281 , 2016
Link: https://doi.org/10.1016/..
 
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13

L'accident ischémique transitoire : une urgence pédiatrique..:

Hubert, Anna ; Curie, Aurore ; Sabatier, Isabelle...
La Presse Médicale.  44 (2015)  2 - p. 249-251 , 2015
Link: https://doi.org/10.1016/..
 
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14

Nevus anemicus in neurofibromatosis type 1: A potential new..:

Marque, Myriam ; Roubertie, Agathe ; Jaussent, Audrey...
Journal of the American Academy of Dermatology.  69 (2013)  5 - p. 768-775 , 2013
Link: https://doi.org/10.1016/..
 
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15

Similar early characteristics but variable neurological out..:

Milh, Mathieu ; Boutry-Kryza, Nadia ; Sutera-Sardo, Julie...
Orphanet Journal of Rare Diseases.  8 (2013)  1 - p. 80 , 2013
Link: https://doi.org/10.1186/..
 
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