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1
Oculopalpebral and facial synkinesis associated with ptosis: epidemiological, clinical, and therapeutic features
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Article
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Oculopalpebral and facial synkinesis associated with ptosis: epidemiological, clinical, and therapeutic features

Journal francais d'ophtalmologie, 2011-02, Vol.34 (2), p.95-107 [Peer Reviewed Journal]

Copyright © 2011. Published by Elsevier Masson SAS. ;EISSN: 1773-0597 ;DOI: 10.1016/j.jfo.2010.10.009 ;PMID: 21277047

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2
Epidemiologic and developmental aspects of congenital cardiopathies in the Sfax pediatric service: 123 cases
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Article
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Epidemiologic and developmental aspects of congenital cardiopathies in the Sfax pediatric service: 123 cases

Tunisie Medicale, 1999-05, Vol.77 (5), p.264-271 [Peer Reviewed Journal]

ISSN: 0041-4131 ;PMID: 10516811

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3
Alopecia, congenital ichthyosis, and growth delay, what is the diagnosis?
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Article
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Alopecia, congenital ichthyosis, and growth delay, what is the diagnosis?

Archives de pédiatrie : organe officiel de la Société française de pédiatrie, 2010-12, Vol.17 (12), p.1685 [Peer Reviewed Journal]

EISSN: 1769-664X ;DOI: 10.1016/j.arcped.2010.09.019 ;PMID: 21036561

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4
Serotonin and the cardiovascular system: role of the serotoninergic 5-HT 2B receptor
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Article
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Serotonin and the cardiovascular system: role of the serotoninergic 5-HT 2B receptor

Bulletin de l'Académie nationale de médecine, 2003, Vol.187 (1), p.117-25; discussion 125-7 [Peer Reviewed Journal]

ISSN: 0001-4079 ;PMID: 14556458

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5
A new type of periodic paralysis: Andersen-Tawil syndrome
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Article
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A new type of periodic paralysis: Andersen-Tawil syndrome

Bulletin de l'Académie nationale de médecine, 2008-11, Vol.192 (8), p.1551-6; discussion 1556-7 [Peer Reviewed Journal]

ISSN: 0001-4079 ;PMID: 19445372

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6
Pseudo-inherited form of left heart obstructive defects revealing maternal phenylketonuria
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Article
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Pseudo-inherited form of left heart obstructive defects revealing maternal phenylketonuria

Archives des maladies du coeur et des vaisseaux, 2000-05, Vol.93 (5), p.649

ISSN: 0003-9683 ;PMID: 10858866

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