Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment von Mkaouar, Rahma, Riahi, Zied, Charfeddine, Cherine, Chelly, Imen, Boudabbous, Hela, Dallali, Hamza, Bonnet, Crystel, Hechmi, Meriem, Bekri, Soumeya, Zitouna, Nadia, Zekri, Lotfi, Tounsi, Amel, Kefi, Rym, Marrakchi, Jihene, Messaoud, Olfa, Kraoua, Ichraf, Maalej, Sonia, Ben Youssef, Ilhem Turki, Ben Hmid, Ahlem, Giraudet, Fabrice, Bouchoucha, Sami, Tebib, Neji, Besbes, Ghazi, Petit, Christine, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha

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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health von Mkaouar, Rahma, Riahi, Zied, Marrakchi, Jihene, Mezzi, Nessrine, Romdhane, Lilia, Boujemaa, Maroua, Dallali, Hamza, Sayeb, Marwa, Lahbib, Saida, Jaouadi, Hajer, Boudabbous, Hela, Zekri, Lotfi, Chargui, Mariem, Messaoud, Olfa, Elyounsi, Meriem, Kraoua, Ichraf, Zaouak, Anissa, Turki, Ilhem, Mokni, Mourad, Boucher, Sophie, Petit, Christine, Giraudet, Fabrice, Mbarek, Chiraz, Besbes, Ghazi, Halayem, Soumeyya, Zainine, Rim, Turki, Hamida, Tounsi, Amel, Bonnet, Crystel, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha, Charfeddine, Cherine

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Letter to the editor: “A case of Guillain-Barré syndrome with meningeal irritation” von Rebai, Ibtihel, Ben Achour, Nedia, El Mabrouk, Emna, Kraoua, Ichraf, Ben Youssef-Turki, Ilhem

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Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood von Rebai, Ibtihel, Ben Rhouma, Hanene, Kraoua, Ichraf, Klaa, Hedia, Rouissi, Aida, Ben Youssef-Turki, Ilhem, Gouider-Khouja, Neziha

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Rasmussen’s Encephalitis: A Report of a Tunisian Pediatric Case and Literature Review von Ben Youssef-Turki, Ilhem, Rouissi, Aida, Nagi, Sonia, Benrhouma, Hanene, Ben Younes, Thouraya, Klaa, Hedia, Kraoua, Ichraf

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Les portes d’entrée neurologiques dans les maladies métaboliques von Ichraf, Kraoua

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Reply to Dr. Suresh Kumar von Ichraf, Kraoua, Neziha, Gouider-Khouja

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Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia von Kraoua, Ichraf, Karkar, Adnane, Drissi, Cyrine, Benrhouma, Hanene, Klaa, Hedia, Samaan, Simon, Renaldo, Florence, Elmaleh, Monique, Ben Hamouda, Mohamed, Abdelhak, Sonia, Boespflug‐Tanguy, Odile, Ben Youssef‐Turki, Ilfghem, Dorboz, Imen

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Parkinsonism in Gaucher's disease type 1: Ten new cases and a review of the literature von Kraoua, Ichraf, Stirnemann, Jérôme, Ribeiro, Maria João, Rouaud, Tiphaine, Verin, Marc, Annic, Agnès, Rose, Christian, Defebvre, Luc, Réménieras, Liliane, Schüpbach, Michaël, Belmatoug, Nadia, Vidailhet, Marie, Sedel, Frédéric

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Supplementation with nicotinamide limits accelerated aging in affected individuals with cockayne syndrome and restores antioxidant defenses von Chikhaoui, Asma, Zayoud, Kouloud, Kraoua, Ichraf, Bouchoucha, Sami, Tebourbi, Anis, Turki, Ilhem, Yacoub-Youssef, Houda

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Subacute sclerosing panencephalitis: Clinical and paraclinical study of Tunisian pediatric cases von Mammou, Syrine Ben, Younes, Thouraya Ben, Miladi, Zouhour, Jemai, Khaoula, Zioudi, Abir, Rouissi, Aida, Klaa, Hedia, Kraoua, Ichraf, Benrhouma, Hanene, Turki, Ilhem Ben Youssef

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MPC2 variants disrupt mitochondrial pyruvate metabolism and cause an early-onset mitochondriopathy von Pujol, Claire, Lebigot, Elise, Gaignard, Pauline, Galai, Said, Kraoua, Ichraf, Bault, Jean-Philippe, Dard, Rodolphe, Youssef-Turki, Ilhem Ben, Omar, Souheil, Boutron, Audrey, Wai, Timothy, Slama, Abdelhamid

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Epidemiological, clinical and paraclinical characteristics of neurodegeneration with brain iron accumulation in childhood von Jemai, Khaoula, Rhouma, Hanene Ben, Kraoua, Ichraf, Rouissi, Aida, Youness, Thouraya Ben, Klaa, Hedia, Turki, Ilhem Ben Youssef

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Pediatric Neurotuberculosis: A cases series and review of the literature von Jamoussi, Maha, Benrhouma, Hanene, Miladi, Zouhour, Ben Younes, Thouraya, Klaa, Hedia, Rouissi, Aïda, Kraoua, Ichraf, Ben Youssef, Ilhem

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Disease Progression in Tunisian Pediatric Multiple Sclerosis von Gharsallah, Farah, Benrhouma, Hanene, Benyounes, Thouraya, Miladi, Zouhour, Zioudi, Abir, Kraoua, Ichraf, Benyoussef-Turki, Ilhem

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Pediatric Onset Multiple Sclerosis: Evaluation of Disease Activity in a Tunisian Cohort von Gharsallah, Farah, Benrhouma, Hanene, Benyounes, Thouraya, Miladi, Zouhour, Zioudi, Abir, Kraoua, Ichraf, Benyoussef-Turki, Ilhem

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Aggressive Pediatric Multiple Sclerosis: Features and therapeutic Challenges von Gharsallah, Farah, Benrhouma, Hanene, Miladi, Zouhour, Benyounes, Thouraya, Klaa, Hedia, Kraoua, Ichraf, Turki, Ilhem Youssef

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Severe dysautonomia as a main feature of anti-GAD encephalitis: Report of a paediatric case and literature review von Ben Achour, Nedia, Ben Younes, Thouraya, Rebai, Ibtihel, Ben Ahmed, Melika, Kraoua, Ichraf, Ben Youssef–Turki, Ilhem

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Mutations in CEP120 cause Joubert syndrome as well as complex ciliopathy phenotypes von Roosing, Susanne, Romani, Marta, Isrie, Mala, Rosti, Rasim Ozgur, Micalizzi, Alessia, Musaev, Damir, Mazza, Tommaso, Al-gazali, Lihadh, Altunoglu, Umut, Boltshauser, Eugen, D'Arrigo, Stefano, De Keersmaecker, Bart, Kayserili, Hülya, Brandenberger, Sarah, Kraoua, Ichraf, Mark, Paul R, McKanna, Trudy, Van Keirsbilck, Joachim, Moerman, Philippe, Poretti, Andrea, Puri, Ratna, Van Esch, Hilde, Gleeson, Joseph G, Valente, Enza Maria

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Differentiating Acute Infectious and Post-Infectious Cerebellitis: A Tunisian Pediatric Case Series von Jamoussi, Maha, Benrhouma, Hanene, Miladi, Zouhour, Younes, Thouraya Ben, Klaa, Hedia, Rouissi, Aida, Kraoua, Ichraf, Youssef, Ilhem Ben

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