Результаты поиска - BENRHOUMA, Hanene

A Case of Progressive Chorea Resulting From GLUT1 Deficiency по Kraoua, Ichraf, Benrhouma, Hanene, Vuillaumier‐Barrot, Sandrine, Klaa, Hedia, Youssef‐Turki, Ilhem Ben

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Mirror Movements and Myelomeningocele: Report of A Single Case and Review of Literature по RéBAI, Ibtihel, BENRHOUMA, Hanene, KRAOUA, Ichraf, DRISSI, Cyrine, Ben HAMMOUDA, Mohammed, GOUIDER-KHOUJA, Neziha

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Mixed movement disorders revealing an atypical form of creatine deficiency syndrome по Nasrallah, Fahmi, Benrhouma, Hanene, Kraoua, Ichraf, Briand, Gilbert, Omar, Souheil, Turki Ben Youssef, Ilhem, Kaabachi, Naziha

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

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Pediatric Multiple Sclerosis in Tunisia: A Retrospective Study over 11 Years по Ben Achour, Nedia, Rebai, Ibtihel, Raddadi, Sarra, Benrhouma, Hanene, Klaa, Hedia, Rouissi, Aida, Kraoua, Ichraf, Ben Youssef Turki, Ilhem

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Autoimmune Encephalitis in Tunisia: Report of a Pediatric Cohort по Douma, Bissene, Ben Younes, Thouraya, Benrhouma, Hanene, Miladi, Zouhour, Zamali, Imen, Rouissi, Aida, Klaa, Hedia, Kraoua, Ichraf, Ben Ahmed, Melika, Ben Youssef Turki, Ilhem

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Novel POLR1C mutation in RNA polymerase III‐related leukodystrophy with severe myoclonus and dystonia по 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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