Pediatric Epilepsy Pioneers and Educational Programs in Kuwait

Suggested Reading
1 Al Tawari A, Ouvrier RA, Steinberg AW, Smith PG, Antony J. Vertebrobasilar Strokes in Children. Med Princ Pract 2000; 9: 186-193
2 Al Tawari A, Ramadan DG, Neubauer D, Heberle LC, Al Awadi F. An early onset form of methylenetetrahydrofolate reductase deficiency: a report of a family from Kuwait. Brain Dev 2002; 24 (05) 304-309
3 Ismail EAR, Shabani IS, Badawi M. , et al. An epidemiologic, clinical, and therapeutic study of childhood Guillain-Barré syndrome in Kuwait: is it related to the oral polio vaccine?. J Child Neurol 1998; 13 (10) 488-492
4 Heberle LC, Ki Abdulla J, Al Tawari A, Al Othman N, Al Mazidi Z. Peroxisomal Disorders: Short review with four case reports. KMJ 2001; 33 (04) 348-352
5 Ramadan DG, Head RA, Al-Tawari A. , et al. Lactic acidosis and developmental delay due to deficiency of E3 binding protein (protein X) of the pyruvate dehydrogenase complex. J Inherit Metab Dis 2004; 27 (04) 477-485
6 Al Tawari A, Al Torki N, Heberle LC. , et al. Newly described multiple congenital anomalies in methyelenetetrahydrofolate reductase deficiency in Arab child. In: The 9th International Child Neurology Congress; Beijing, China; September 20–25; 2002; Brain & Development 2000;24(6):563
7 Nanda A, Lionel J, Al-Tawari AA, Anim JT. What syndrome is this? Autosomal recessive type II cutis laxa. Pediatr Dermatol 2004; 21 (02) 166-169
8 Dixon-Salazar T, Silhavy JL, Marsh SE. , et al. Mutations in the AHI1 gene, encoding jouberin, cause Joubert syndrome with cortical polymicrogyria. Am J Hum Genet 2004; 75 (06) 979-987
9 Valente EM, Marsh SE, Castori M. , et al. Distinguishing the four genetic causes of Jouberts syndrome-related disorders. Ann Neurol 2005; 57 (04) 513-519
10 Haider MZ, Habeeb Y, Al-Nakkas E. , et al. Lack of an association between candidate gene loci and idiopathic generalized epilepsy in Kuwaiti Arab children. J Biomed Sci 2005; 12 (05) 815-818
11 Heberle LC, Al Tawari AA, Ramadan DG, Ibrahim JK. Ethylmalonic encephalopathy-report of two cases. Brain Dev 2006; 28 (05) 329-331
12 Ibrahim Abdulla JK, Vattoth S, Al Tawari AA, Pandey T, Abubacker S. Brain MRI features of merosin-negative congenital muscular dystrophy. Australas Radiol 2007; 51 (Suppl): B221-B223
13 Pavlović M, Neubauer D, Al Tawari A, Heberle LC. The microcephaly-capillary malformation syndrome in two brothers with novel clinical features. Pediatr Neurol 2014; 51 (04) 560-565
14 Pavlović MV, Jarebinski MS, Pekmezović TD, Marjanovic BD, Levic ZM. Febrile convulsions in a Serbian region: a 10-year epidemiological study. Eur J Neurol 1999; 6 (01) 39-42
15 Pavlović M, Jarebinski M, Pekmezović T, Levic Z. Seizure disorders in preschool children in a Serbian district. Neuroepidemiology 1998; 17 (02) 105-110
16 Pavlovic MV, Jarebinski MS, Pekmezovic TD, Janicijevic MA. Risk factors from brain tumors in children and adolescents: a case-control study in Belgrade, Serbia. Eur J Neurol 2005; 12 (07) 508-513
17 Pavlović M, Jović N, Pekmezović T. Antiepileptic drugs withdrawal in patients with idiopathic generalized epilepsy. Seizure 2011; 20 (07) 520-525
18 Pavlović M, Jović N, Pekmezović T. Withdrawal of antiepileptic drugs in young patients with cryptogenic focal epilepsies. Seizure 2012; 21 (06) 431-436
19 Pavlović M, Neubauer D, Al Tawari A, Heberle LC. The microcephaly-capillary malformation syndrome in two brothers with novel clinical features. Pediatr Neurol 2014; 51 (04) 560-565
20 Lamberink HJ, Otte WM, Geerts AT. , et al. Individualised prediction model of seizure recurrence and long-term outcomes after withdrawal of antiepileptic drugs in seizure-free patients: a systematic review and individual participant data meta-analysis. Lancet Neurol 2017; 16 (07) 523-531