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1. • Speech

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   Idiopathic pulmonary arterial hypertension in infancy: Rule out NFU1 deficiency

   Paquay, Stéphanie[UCL] Sluysmans, Thierry[UCL] Loeckx, Isabelle Sznajer, Yves[UCL] Vachiery, Jean-Luc Seneca, Sara Nassogne, Marie-Cécile[UCL] (2017) Belgian Society of Pediatric Neurology — Bruges
2. • Speech

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   Uncommon Leber "plus" disease associated with mitochondrial m.11778G>A mutation in a premature child

   Paquay, Stéphanie[UCL] Benoit, Valérie Wetzburger, Catherine Cordonnier, Monique Meire, Françoise Charon, Anne Roland, Dominique Van Coster, Rudy Nassogne, Marie-Cécile[UCL] Maystadt, Isabelle (2013) Belgian Society of Pediatric Neurology — Luxembourg
3. • Journal article

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   A novel splicing mutation in SLC12A3 associated with Gitelman syndrome and idiopathic intracranial hypertension.

   Godefroid, Nathalie Riveira-Munoz, Eva[UCL] Saint-Martin, Christine Nassogne, Marie-Cécile[UCL] Dahan, Karin[UCL] Devuyst, Olivier[UCL] (2006) American journal of kidney diseases : the official journal of the National Kidney Foundation — Vol. 48, no. 5, p. e73-9 (2006)
4. • Journal article

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   Pediatric diffusion tensor imaging: normal database and observation of the white matter maturation in early childhood.

   Hermoye, Laurent[UCL] Saint-Martin, Christine[UCL] Cosnard, Guy[UCL] Lee, Seung-Koo Kim, Jinna Nassogne, Marie-Cécile[UCL] Menten, Renaud[UCL] Clapuyt, Philippe[UCL] Donohue, Pamela K Hua, Kegang Wakana, Setsu Jiang, Hangyi van Zijl, Peter C M Mori, Susumu (2006) NeuroImage — Vol. 29, no. 2, p. 493-504 (2006)
5. • Journal article

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   Molecular identification of aspartate N-acetyltransferase and its mutation in hypoacetylaspartia

   Wiame, Elsa[UCL] Tyteca, Donatienne[UCL] Pierrot, Nathalie[UCL] Collard, François[UCL] Amyere, Mustapha[UCL] Noël, Gaëtane[UCL] Desmedt, Jonathan[UCL] Nassogne, Marie-Cécile[UCL] Vikkula, Miikka[UCL] Octave, Jean-Noël[UCL] Vincent, Marie-Françoise[UCL] Courtoy, Pierre J.[UCL] Boltshauser, Eugen Van Schaftingen, Emile[UCL] (2010) Biochemical Journal — Vol. 425, no. 1, p. 127-136 (2010)
6. • Journal article

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   Treatment and long term outcome in West syndrome: The clinical reality. A multicentre follow up study

   Lagae, Lieven[UCL] Nassogne, Marie-Cécile[UCL] Verhelst, Helene Ceulemans, Berten De Meirleir, Linda De Borchgrave, Valerie D'Hooghe, Marc Foulon, Martine Van Bogaert, Patrick (2010) Seizure - European Journal of Epilepsy — Vol. 19, no. 3, p. 159-64 (2010)
7. • Journal article

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   Mutation of a nuclear respiratory factor 2 binding site in the 5' untranslated region of the ADSL gene in three patients with adenylosuccinate lyase deficiency.

   Marie, S. Race, V Nassogne, Marie-Cécile[UCL] Vincent, Marie-Françoise[UCL] Van den Berghe, Georges[UCL] (2002) American journal of human genetics — Vol. 71, no. 1, p. 14-21 (2002)
8. • Journal article

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   L-2-Hydroxyglutaric aciduria: clinical, genetic, and brain MRI characteristics in two adult sisters.

   Goffette, Sophie[UCL] Duprez, Thierry[UCL] Nassogne, Marie-Cécile[UCL] Vincent, M-F A[UCL] Jakobs, C. Sindic, Christian[UCL] (2006) European Journal of Neurology — Vol. 13, no. 5, p. 499-504 (2006)
9. • Journal article

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   Selective neuronal toxicity of cocaine in embryonic mouse brain cocultures.

   Nassogne, Marie-Cécile[UCL] Courtoy, Pierre J.[UCL] Evrard, Philippe[UCL] (1995) Proceedings of the National Academy of Sciences of the United States of America — Vol. 92, no. 24, p. 11029-33 (1995)
10. • Journal article

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    In vitro neuroteratogenicity of valproic acid and 4-en-VPA

    Gofflot, Françoise[UCL] Nassogne, Marie-Cécile[UCL] Etzion, T. Van Maele, Geneviève[UCL] Evrard, Philippe[UCL] Picard, Jacques[UCL] (1995) Neurotoxicology and Teratology — Vol. 17, no. 4, p. 425-435 (1995)
11. • Journal article

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    HUWE1 variants cause dominant X-linked intellectual disability: a clinical study of 21 patients.

    Moortgat, Stéphanie Berland, Siren Aukrust, Ingvild Maystadt, Isabelle Baker, Laura Benoit, Valerie Caro-Llopis, Alfonso Cooper, Nicola S Debray, François-Guillaume Faivre, Laurence Gardeitchik, Thatjana Haukanes, Bjørn I Houge, Gunnar Kivuva, Emma Martinez, Francisco Mehta, Sarju G Nassogne, Marie-Cécile[UCL] Powell-Hamilton, Nina Pfundt, Rolph Rosello, Monica Prescott, Trine Vasudevan, Pradeep van Loon, Barbara Verellen-Dumoulin, Christine Verloes, Alain Lippe, Charlotte von der Wakeling, Emma Wilkie, Andrew O M Wilson, Louise Yuen, Amy Study, Ddd Low, Karen J Newbury-Ecob, Ruth A (2018) European Journal of Human Genetics — Vol. 26, no. 1, p. 64-74 (2018)
12. • Journal article

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    Decreased plasma l-arginine levels in organic acidurias (MMA and PA) and decreased plasma branched-chain amino acid levels in urea cycle disorders as a potential cause of growth retardation: Options for treatment.

    Molema, Femke Gleich, Florian Burgard, Peter van der Ploeg, Ans T Summar, Marshall L Chapman, Kimberly A Lund, Allan M Rizopoulos, Dimitris Kölker, Stefan Williams, Monique Additional individual contributors from E-IMD Sokal, Etienne[UCL] Nassogne, Marie-Cécile[UCL] (2019) Molecular genetics and metabolism — Vol. 126, no. 4, p. 397-405 (2019)
13. • Dissertation

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    Cocaine induces apoptosis in embryonic mouse neurons : teratogenic implications

    Nassogne, Marie-Cécile[UCL] (1997)
14. • Journal article

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    Megalencephalic leukoencephalopathy with subcortical cysts: Characterization of disease variants.

    Hamilton, Eline M C Tekturk, Pinar Cialdella, Fia van Rappard, Diane F Wolf, Nicole I Yalcinkaya, Cengiz Çetinçelik, Ümran Rajaee, Ahmad Kariminejad, Ariana Paprocka, Justyna Yapici, Zuhal Bošnjak, Vlatka Mejaški van der Knaap, Marjo S MLC Research Group Nassogne, Marie-Cécile[UCL] (2018) Neurology — Vol. 90, no. 16, p. e1395-e1403 (2018)
15. • Journal article

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    Evaluation of dietary treatment and amino acid supplementation in organic acidurias and urea-cycle disorders

    Molema, Femke Gleich, Florian Burgard, Peter van der Ploeg, Ans T. Summar, Marshall L. Chapman, Kimberly A. Barić, Ivo Lund, Allan M. Kölker, Stefan Williams, Monique Additional individual contributors from E-IMD Sokal, Etienne[UCL] Nassogne, Marie-Cécile[UCL] (2019) Journal of Inherited Metabolic Disease — Vol. 42, no. 6, p. 1162-1175 (2019)
16. • Speech

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    Succès de la greffe hepatique dans la leucinose selon un protocole belgo-suisse

    ROCK, Nathalie[UCL] McLin, Valérie Stéphenne, Xavier[UCL] Witters, Peter Morava, Eva[UCL] Wildhaber, Barbara De Magnee, Catherine[UCL] Reding, Raymond[UCL] Kern, Ilse Nassogne, Marie-Cécile[UCL] Sokal, Etienne[UCL] (2018) SFEIM (Société Française pour l'Etude des Erreurs Innées du Métabolisme) — Bruxelles, Belgique
17. • Journal article

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    Hydrocephalus in children under the age of five from diagnosis to short-/medium-/long-term progression: a retrospective review of 142 children.

    Perdaens, Océane[UCL] Koerts, Guus[UCL] Nassogne, Marie-Cécile[UCL] (2018) Acta Neurologica Belgica — Vol. 118, no. 1, p. 97-103 (2018)
18. • Journal article

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    Pseudotumoral cerebellitis with acute hydrocephalus as a manifestation of EBV infection.

    Geurten, Claire De Bilderling, Georges[UCL] Nassogne, Marie-Cécile[UCL] Misson, Jean-Paul Verghote, Marc (2018) Revue Neurologique — Vol. 174, no. 1-2, p. 70-72 (2018)
19. • Journal article

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    Pancreatic arterial calcium stimulation in the diagnosis and localisation of persistent hyperinsulinemic hypoglycaemia of infancy.

    Chigot, V De Lonlay, P Nassogne, Marie-Cécile[UCL] Laborde, K Delagne, V Fournet, J C Nihoul-Fékété, C Saudubray, J M Brunelle, F (2001) Pediatric radiology — Vol. 31, no.9, p. 650-655 (2001)
20. • BookChapter

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    Les maladies métaboliques héréditaires du système nerveux : Chapitre XXXVI, La neurologie de l’enfant

    Nassogne, Marie-Cécile[UCL] Laterre, Emile-Christian[UCL] (2008) Sémiologie des maladies nerveuses — [ISBN : 9782804156916]
21. • Journal article

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    Stroke et pseudo-stroke d'origine héréditaire métabolique à l'âge adulte

    Nassogne, Marie-Cécile[UCL] Touati, G Beyler, C Saudubray, J M (2001) La Revue de médecine interne — Vol. 22 Suppl 3, p. 338s-346s (2001)
22. • Journal article

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    Imparaid mitochondrial pyruvate importation in a patient and a fetus at risk

    Brivet, M Garcia-Cazorla, A Lyonnet, S Dumez, Y Nassogne, Marie-Cécile[UCL] Slama, A Boutron, A Touati, G Legrand, A Sandubray, JM (2003) Molecular Genetics and Metabolism — Vol. 78, no.3, p. 186-192 (2003)
23. • Journal article

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    Atypical phenotype? The answer’s in the genotype: AGS caused by a novel RNASEH2C variant combined with XLA caused by a BTK deficiency.

    Boulanger, Cécile[UCL] Chatzis, Olga[UCL] Nolf, Delphine[UCL] Brichard, Bénédicte[UCL] Lauwerys, Bernard[UCL] Nassogne, Marie-Cécile[UCL] Limaye, Nisha[UCL] (2021) Rheumatology — Vol. 60, no. 7, p. e240-e242 (2021)
24. • Journal article

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    Chudley-McCullough Syndrome: A Recognizable Clinical Entity Characterized by Deafness and Typical Brain Malformations.

    Blauen, Aglaé[UCL] Stutterd, Chloe A Stouffs, Katrien Dumitriu, Dana Ioana[UCL] Deggouj, Naima[UCL] Lockhart, Paul J Leventer, Richard J Nassogne, Marie-Cécile[UCL] Jansen, Anna C (2021) Journal of child neurology — Vol. 36, no. 2, p. 152-158 (2021)
25. • Journal article

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    Coma postopératoire chez une jeune fille

    Nassogne, Marie-Cécile[UCL] Veyckemans, Francis[UCL] (2008) Percentile — Vol. 13, no.4, p. 167-169 (2008)

Pages