Benrhouma H - Search Results

1

Neuronal ceroïd-lipofuscinosis: Clinical, electroencephalographic, imaging, and genetic study of a maghrebian series.

Ben Younes T, Kraoua I, Snanoudj S, Klaa H, Benrhouma H, Rouissi A, Caillaud C, Chaabouni M, Miladi N, Bekri S, Ben Youssef-Turki I. Ben Younes T, et al. Among authors: benrhouma h. Clin Genet. 2022 Aug;102(2):157-160. doi: 10.1111/cge.14145. Clin Genet. 2022. PMID: 35796208

2

Movement disorders in neuro-metabolic diseases.

Gouider-Khouja N, Kraoua I, Benrhouma H, Fraj N, Rouissi A. Gouider-Khouja N, et al. Among authors: benrhouma h. Eur J Paediatr Neurol. 2010 Jul;14(4):304-7. doi: 10.1016/j.ejpn.2009.11.005. Epub 2009 Dec 16. Eur J Paediatr Neurol. 2010. PMID: 20015670 Review.

3

Lesch Nyhan syndrome: a novel complex mutation in a Tunisian child.

Rebai I, Kraoua I, Benrhouma H, Rouissi A, Turki I, Ceballos-Picot I, Gouider-Khouja N. Rebai I, et al. Among authors: benrhouma h. Brain Dev. 2014 Nov;36(10):921-3. doi: 10.1016/j.braindev.2014.01.006. Epub 2014 Feb 3. Brain Dev. 2014. PMID: 24503445

4

Mirror movements and myelomeningocele: report of a single case and review of literature.

Rébai I, Benrhouma H, Kraoua I, Drissi C, Ben Hammouda M, Gouider-Khouja N. Rébai I, et al. Among authors: benrhouma h. Iran J Child Neurol. 2013 Summer;7(3):58-61. Iran J Child Neurol. 2013. PMID: 24665308 Free PMC article.

5

Postencephalitic parkinsonism and selective involvement of substantia nigra in childhood.

Rebai I, Ben Rhouma H, Kraoua I, Klaa H, Rouissi A, Ben Youssef-Turki I, Gouider-Khouja N. Rebai I, et al. Brain Dev. 2015 Jan;37(1):153-7. doi: 10.1016/j.braindev.2014.03.009. Epub 2014 Apr 16. Brain Dev. 2015. PMID: 24745788 Review.

6

Mixed movements disorders as an initial feature of pediatric lupus.

Mrabet S, Benrhouma H, Kraoua I, Naas A, Achour NB, Klaa H, Turki I. Mrabet S, et al. Among authors: benrhouma h. Brain Dev. 2015 Oct;37(9):904-6. doi: 10.1016/j.braindev.2015.01.008. Epub 2015 Feb 28. Brain Dev. 2015. PMID: 25736974

7

Mixed movement disorders revealing an atypical form of creatine deficiency syndrome.

Nasrallah F, Benrhouma H, Kraoua I, Briand G, Omar S, Turki Ben Youssef I, Kaabachi N. Nasrallah F, et al. Among authors: benrhouma h. Iran J Neurol. 2015 Jan 5;14(1):47-9. Iran J Neurol. 2015. PMID: 25874057 Free PMC article. No abstract available.

8

Anti-Ma2-encephalitis in a 2 year-old child: A newly diagnosed case and literature review.

Mrabet S, Ben Achour N, Kraoua I, Benrhouma H, Klaa H, Rouissi A, Ben Ahmed M, Ben Youssef Turki I. Mrabet S, et al. Among authors: benrhouma h. Eur J Paediatr Neurol. 2015 Nov;19(6):737-42. doi: 10.1016/j.ejpn.2015.06.005. Epub 2015 Jul 9. Eur J Paediatr Neurol. 2015. PMID: 26190012

9

Status dystonicus in childhood.

Touati N, Ben Rhouma H, Kraoua I, Klaa H, Turki I, Gouider-Khouja N. Touati N, et al. Tunis Med. 2015 Dec;93(12):756-9. Tunis Med. 2015. PMID: 27249384

10

Childhood opsoclonus-myoclonus syndrome: A case series from Tunisia.

Ben Achour N, Mrabet S, Rebai I, Abid I, Benrhouma H, Klaa H, Rouissi A, Kraoua I, Ben Youssef Turki I. Ben Achour N, et al. Among authors: benrhouma h. Brain Dev. 2017 Oct;39(9):751-755. doi: 10.1016/j.braindev.2017.05.001. Epub 2017 May 23. Brain Dev. 2017. PMID: 28549713

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