Search Results - "Laroussi, N."

Pregnancy After Heart Transplantation: A Well-Thought-Out Decision? by Dagher, O, Laroussi, N, Cantin, B, Carrier, M, Cecere, R, Charbonneau, E, De Denus, S, Giannetti, N, Leduc, L, Levesque, S, Poirier, N, Raboisson, M, White, M, Ducharme, A

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Clinical and molecular investigation of Buschke-Fischer-Brauer in consanguineous Tunisian families by Charfeddine, C., Ktaifi, C., Laroussi, N., Hammami, H., Jmel, H., Landoulsi, Z., Badri, T., Benmously, R., Bchetnia, M., Boubaker, M.S., Fenniche, S., Abdelhak, S., Mokni, M.

“…Background Punctate palmoplantar keratoderma type I (PPPK‐BFB), also called Buschke‐Fischer‐Brauer disease (MIM 148600) is a rare autosomal dominant disorder…”
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OUTCOMES IN CHILDREN LISTED IN TOTAL RENAL FAILURE FOR HEART TRANSPLANT by Alami Laroussi, N, Gowrishankar, M, Conway, J, Kantor, P, Ross, D, Rebeyka, I, West, L, Urschel, S

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Genetic basis of dominant dystrophic epidermolysis bullosa in tunisian families and co-occurrence of dominant and recessive mutations by Ben Brick, A.S., Laroussi, N., Mesrati, H., Kefi, R., Ouragini, H., Bchetnia, M., Romdhane, L., Marrakchi, S., Boubaker, M.S., Castiglia, D., Hovnanian, A., Abdelhak, S., Turki, H., Kharfi, M.

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The experience of a Tunisian referral centre in prenatal diagnosis of Xeroderma pigmentosum by Messaoud, O, Ben Rekaya, M, Jerbi, M, Ouertani, I, Kefi, R, Laroussi, N, Bouyacoub, Y, Benfadhel, S, Yacoub-Youssef, H, Boubaker, S, Zghal, M, Mrad, R, Amouri, A, Abdelhak, S

“…Xeroderma pigmentosum (XP, OMIM 278700-278780) is one of the most severe genodermatoses and is relatively frequent in Tunisia. In the absence of any therapy…”
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(1338) - Perception vs. Reality: Reported and Objective Measures of Physical Activity in Children with Hypertrophic Cardiomyopathy (HCM) by Fortin-Moore, C., Jeewa, A., Lemaire-Paquette, S., Pidborochynski, T., Khoury, M., Cunningham, C., Dhillon, S., Alami Laroussi, N., Vaujois, L., Dallaire, F., Armstrong, K., Schantz, D., Mawad, W., Bradley, T., Conway, J.

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Mercury and polychlorinated biphenyls in zooplankton and shrimp from the Barents Sea and the Spitsbergen area by Joiris, C.R. (Free University of Brussels, Brussels, Belgium.), Moatemri, N.L, Holsbeek, L

“…Zooplankton and the shrimp Pandalus borealis were sampled during 2 cruises in 1991. Subsamples were acid digested and analysed for mercury by atomic absorption…”
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Mercury and polychlorinated biphenyls in suspended particulate matter from the European Arctic seas by JOIRIS, C. R, LAROUSSI MOATEMRI, N, HOLSBEEK, L

“…The concentration of mercury and PCB was determined in the particulate matter from the Greenland sea, Barents sea and the Arctic basin between June and October…”
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048 Aortic Dilation in Patients With Turner Syndrome by Laroussi, N. Alami, Fournier, A, Thérien, J, Dahdah, N

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Profil génétique des épidermolyses bulleuses dystrophiques généralisées récessives (EBDR-GS) à Sfax (centre-est tunisien) by Sellami, K., Mesrati, H., Laroussi, N., Abdessalem, G., Marrakchi, S., Abdelhak, S., Masmoudi, A., Turki, H.

“…La prévalence des épidermolyses bulleuses dystrophiques généralisées récessives (EBDR-GS) à Sfax (centre-est tunisien) est considérée élevée…”
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Identification of a Novel Mutation of LAMB3 Gene in a Lybian Patient with Hereditary Epidermolysis Bullosa by Whole Exome Sequencing by Laroussi, Nadia, Messaoud, Olfa, Chargui, Mariem, Ben Fayala, Chaima, Elahlafi, Abdelaziz, Mokni, Mourad, Bashamboo, Anu, McElreavey, Kenneth, Boubaker, Mohamed Samir, Yacoub Youssef, Houda, Abdelhak, Sonia

“…In this study, we carried out whole exome sequencing (WES) analysis in one Libyan patient in order to identify the molecular aetiology of hereditary…”
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Mortalité au cours des épidermolyses bulleuses héréditaires dystrophiques : notre expérience by Sellami, K., Mesrati, H., Marrakchi, S., Laroussi, N., Abdessalem, G., Abdelhak, S., Bali, N., Mseddi, M., Masmoudi, A., Turki, H.

“…Les épidermolyses bulleuses (EB) dystrophiques (EBD) peuvent être responsables de décès précoce notamment au cours des EBD récessives généralisées sévères…”
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Particularités épidémio-clinique et génétique de l’épidermolyse bulleuse héréditaire : à propos d’une série de 34 cas au centre Tunisien by Korbi, M., Aounallah, A., Laroussi, N., Belajouza, C., Ghariani Fetoui, N., Ghariani, N., Boussofara, L., Saidi, W., Mokni, S., Abdelhak, S., Denguezli, M., Nouira, R.

“…Les épidermolyses bulleuses héréditaires (EBH) constituent un groupe hétérogène de génodermatoses. L’objectif de ce travail consiste à décrire les…”
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Maladies dermatologiques en Algérie by Tiar, A., Romdhane, L., Messaoud, O., Rekaya, M. Ben, Brik, S. Ben, Laroussi, N., Bchetnia, M., Abdelhak, S.

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Développement d’un test de diagnostic moléculaire simple pour le diagnostic moléculaire de Xeroderma pigmentosum de type variant by Ben Rekaya, M., Laroussi, N., Messaoud, O., Jones, M., Jerbi, B.M., Naouali, C., Fazaa, B., Boussen, H., Mokni, M., Abdelhak, S., Zghal, M., Khaled, A., Yacoub-Youssef, H.

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Investigation moléculaire préliminaire des ichtyoses non syndromiques autosomiques récessives en Tunisie by Laroussi, N., Brik, A.S., Messai, H., Zaouak, A., Daoued, L., Bchetnia, M., Kacem, M., Mokni, M., Boubaker, M.-S., Benmously, R., Abdelhak, S.

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Non alcoholic steatohepatitis: a multifactorial, frequent, paucysymptomatic liver disease with a fibrotic outcome by Laroussi, Nadia, Mosnier, Jean-François, Morel, Yves, Deugnier, Yves, Dumas, Olivier, Audigier, Jean-Christian

“…The aim of this study was to evaluate the morphological, clinical and biochemical characteristics of non alcoholic steatohepatitis to understand its…”
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Cervical osteosynthesis for myelopathy: an unusual cause of dysphagia by Laroussi, N, Barthélémy, C, Brunon, J, Audigier, J C

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Cervical osteosynthesis for myelopathy: an unusual cause of dysphagia by Laroussi, N, Barthélémy, C, Brunon, J, Audigier, J C

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