Management of peripheral facial nerve palsy in children von Tabarki, B

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Therapeutic hypothermia in children: Which indications remain in 2018? von Thabet, F., Tabarki, B.

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Cerebral venous sinus thrombosis in children: risk factors, presentation, diagnosis and outcome von Sébire, G., Tabarki, B., Saunders, D. E., Leroy, I., Liesner, R., Saint-Martin, C., Husson, B., Williams, A. N., Wade, A., Kirkham, F. J.

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Inflammatory cytokines in the pathogenesis of periventricular leukomalacia von Kadhim, H, Tabarki, B, Verellen, G, De Prez, C, Rona, A M, Sébire, G

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PPP1R21 homozygous null variants associated with developmental delay, muscle weakness, distinctive facial features, and brain abnormalities von Suleiman, J., Al Hashem, A.M., Tabarki, B., Al‐Thihli, K., Bi, W., El‐Hattab, A.W.

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Vitamin-responsive epilepsies: an update von Tabarki, B, Thabet, F

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Prise en charge de la paralysie faciale périphérique chez l’enfant von Tabarki, B.

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Épilepsies vitamino-sensibles von Tabarki, B., Thabet, F.

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Interleukin-2 in the pathogenesis of perinatal white matter damage von KADHIM, H, TABARKI, B, DE PREZ, C, RONA, A.-M, SEBIRE, G

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Acute cerebellitis with hydrocephalus and brainstem compression von Tabarki Melaiki, B, Thabet, F, Anjum, S B, Amin, A

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Genetic heterogeneity of megalencephalic leukoencephalopathy and subcortical cysts von Patrono, C, Di Giacinto, G, Eymard-Pierre, E, Santorelli, F M, Rodriguez, D, De Stefano, N, Federico, A, Gatti, R, Benigno, V, Megarbané, A, Tabarki, B, Boespflug-Tanguy, O, Bertini, E

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Prolonged electrocerebral depression after oral administration of pyridoxine for pyridoxine-dependent convulsions von Tabarki, B, Thabet, F

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Severe Cerebellar Hypoplasia Associated with Osteogenesis Imperfecta Type III von Tabarki, B., MD, Al-Malki, S., MD, Al-Ghamdi, H., MD

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Thiamine deficiency in childhood with attention to genetic causes: Survival and outcome predictors von Ortigoza‐Escobar, Juan Darío, Alfadhel, Majid, Molero‐Luis, Marta, Darin, Niklas, Spiegel, Ronen, de Coo, Irenaeus F., Gerards, Mike, Taylor, Robert W., Artuch, Rafael, Nashabat, Marwan, Rodríguez‐Pombo, Pilar, Tabarki, Brahim, Pérez‐Dueñas, Belén, Distelmaier, Felix, Hahn, Andreas, Morava, Eva, Banka, Siddharth, Debs, Rabab, Fraser, Jamie L., Isohanni, Pirjo, Lähdesmäki, Tuire, Livingston, John, Nadjar, Yann, Schuler, Elisabeth, Uusimaa, Johanna, Vanderver, Adeline, Friedman, Jennifer R., Zimbric, Michael R., McFarland, Robert, Santra, Saikat, Wassmer, Evangeline, Martí‐Sanchez, Laura, Darling, Alejandra

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Biotin-responsive basal ganglia disease revisited: Clinical, radiologic, and genetic findings von TABARKI, Brahim, AL-SHAFI, Shatha, AL-SHAHWAN, Saad, AZMAT, Zeeshan, AL-HASHEM, Amel, AL-ADWANI, Nawal, BIARY, Nabil, AL-ZAWAHMAH, Mohamed, KHAN, Sonia, ZUCCOLI, Giulio

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Bi-allelic loss-of-function variants in PPFIBP1 cause a neurodevelopmental disorder with microcephaly, epilepsy, and periventricular calcifications von Rosenhahn, Erik, O’Brien, Thomas J., Zaki, Maha S., Sorge, Ina, Wieczorek, Dagmar, Rostasy, Kevin, Vitobello, Antonio, Nambot, Sophie, Alkuraya, Fowzan S., Hashem, Mais O., Alhashem, Amal, Tabarki, Brahim, Alamri, Abdullah S., Al Safar, Ayat H., Bubshait, Dalal K., Alahmady, Nada F., Gleeson, Joseph G., Abdel-Hamid, Mohamed S., Lesko, Nicole, Ygberg, Sofia, Correia, Sandrina P., Wredenberg, Anna, Alavi, Shahryar, Seyedhassani, Seyed M., Ebrahimi Nasab, Mahya, Hussien, Haytham, Omar, Tarek E.I., Harzallah, Ines, Touraine, Renaud, Tajsharghi, Homa, Morsy, Heba, Houlden, Henry, Shahrooei, Mohammad, Ghavideldarestani, Maryam, Abdel-Salam, Ghada M.H., Torella, Annalaura, Zanobio, Mariateresa, Terrone, Gaetano, Brunetti-Pierri, Nicola, Omrani, Abdolmajid, Hentschel, Julia, Lemke, Johannes R., Sticht, Heinrich, Abou Jamra, Rami, Brown, Andre E.X., Maroofian, Reza, Platzer, Konrad

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Steroid therapy for hydrocephalus due to acute cerebellitis in a child von Tabarki, B, Thabet, F

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Critical illness neuromuscular disease: clinical, electrophysiological, and prognostic aspects von Tabarki, B, Coffiniéres, A, Van den Bergh, P, Huault, G, Landrieu, P, Sébire, G

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Acute encephalopathy von Tabarki, B, Thabet, F

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Encéphalopathie aiguë nécrosante à entérovirus de l’enfant von Tabarki, B., Thabet, F.

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