Search Results - Ghomari, Hassan El

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  1. 1
    Apport de l'orientation clinique dans le diagnostic des hypertensions arterielles endocriniennes

    Apport de l'orientation clinique dans le diagnostic des hypertensions arterielles endocriniennes by El Aziz, Siham, Chadli, Asma, Louda, Fatima, El Ghomari, Hassan, Farouqi, Ahmed

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  2. 2
    Pulmonary epidermoid carcinoma in a patient with acromegaly: a rare entity

    Pulmonary epidermoid carcinoma in a patient with acromegaly: a rare entity by El Aziz, Siham, Chadli, Asma, Obbiba, Atika, El Ghomari, Hassan, Farouqi, Ahmed

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  3. 3
    Apport de l’orientation clinique dans le diagnostic des hypertensions arterielles endocriniennes

    Apport de l’orientation clinique dans le diagnostic des hypertensions arterielles endocriniennes by Aziz, Siham El, Chadli, Asma, Louda, Fatima, Ghomari, Hassan El, Farouqi, Ahmed

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    Autosomal recessive hypercholesterolaemia in a Morrocan family due to a mutation of the G266C LDL receptor

    Autosomal recessive hypercholesterolaemia in a Morrocan family due to a mutation of the G266C LDL receptor by El Aziz, Siham, Chadli, Asma, El Ghomari, Hassan, Farouqi, Ahmed

    Published in BMJ case reports
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  5. 5
    Syndrome de Nelson : quelle prise en charge thérapeutique ? (à propos d’un cas et revue de la littérature)

    Syndrome de Nelson : quelle prise en charge thérapeutique ? (à propos d’un cas et revue de la littérature) by Mjabber, Amal, Aziz, Siham El, Chadli, Asmaa, Ghomari, Hassan El, Farouqi, Ahmed

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  6. 6
    Syndrome de Sheehan : à propos de 20 cas

    Syndrome de Sheehan : à propos de 20 cas by Moutaouakil, Amal, Chadli, Asma, El Aziz, Siham, El Ghomari, Hassan, Ahmed, Farouqi

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  7. 7
    Contribution of clinical guidance in the diagnosis of endocrine arterial hypertension

    Contribution of clinical guidance in the diagnosis of endocrine arterial hypertension by El Aziz, Siham, Chadli, Asma, Louda, Fatima, El Ghomari, Hassan, Farouqi, Ahmed

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  8. 8
    Autosomal recessive hypercholesterolaemia in a Morrocan family due to a mutation of the G266C LDL receptor

    Autosomal recessive hypercholesterolaemia in a Morrocan family due to a mutation of the G266C LDL receptor by El Aziz, Siham, Chadli, Asma, El Ghomari, Hassan, Farouqi, Ahmed

    Published in BMJ Case Reports
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