High Frequency of Enterocytozoon bieneusi Genotype WL12 Occurrence among Immunocompromised Patients with Intestinal Microsporidiosis von Messaoud, Mariem, Abbes, Salma, Gnaien, Mayssa, Rebai, Yasmine, Kallel, Aicha, Jemel, Sana, Cherif, Ghaya, Skhairia, Mohamed Amine, Marouen, Sonia, Fakhfekh, Najla, Mardassi, Helmi, Belhadj, Slaheddine, Znaidi, Sadri, Kallel, Kalthoum

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Optimizing pear micropropagation and rooting with light emitting diodes and trans-cinnamic acid von Lotfi, Mariem, Mars, Messaoud, Werbrouck, Stefaan

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First genetic characterization of Xeroderma pigmentosum in Libya: High frequency of XP‐C founder mutation von Khalat, Najlaa, Messaoud, Olfa, Ben Rekaya, Mariem, Chargui, Mariem, Zghal, Mohamed, Zendah, Bashir, Saqer, Najat, Mokni, Mourad, Abdelhak, Sonia, Mohamed, Othman A.

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Effects ofmeta-topolin derivatives and temporary immersion on hyperhydricity and in vitro shoot proliferation inPyrus communis von Lotfi, Mariem, Bayoudh, Chokri, Werbrouck, Stefaan, Mars, Messaoud

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Whole Exome Sequencing allows the identification of two novel groups of Xeroderma pigmentosum in Tunisia, XP-D and XP-E: Impact on molecular diagnosis von Ben Rekaya, Mariem, Naouali, Chokri, Messaoud, Olfa, Jones, Meriem, Bouyacoub, Yosra, Nagara, Majdi, Pippucci, Tommaso, Jmel, Haifa, Chargui, Mariem, Jerbi, Manel, Alibi, Mohamed, Dallali, Hamza, Bashamboo, Anu, McElreavey, Kenneth, Romeo, Giovanni, Barakat, Abdelhamid, Zghal, Mohamed, Yacoub-Youssef, Houda, Abdelhak, Sonia

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Effects of meta–topolin derivatives and temporary immersion on hyperhydricity and in vitro shoot proliferation in Pyrus communis von Lotfi, Mariem, Bayoudh, Chokri, Werbrouck, Stefaan, Mars, Messaoud

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Role of vitamin D receptor polymorphism in multiple sclerosis disease course von Jamoussi, Maha, Alaya, Faten, Jamoussi, Hela, Baraket, Ghada, Achouri, Afef, Mahmoud, Mariem Ben, Fray, Saloua, Ali, Nadia Ben, Messaoud, Taieb, Hannachi, Amal, Fradj, Mohamed

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Corrigendum: Current phenotypic and genetic spectrum of syndromic deafness in Tunisia: paving the way for precision auditory health von Mkaouar, Rahma, Riahi, Zied, Marrakchi, Jihene, Mezzi, Nessrine, Romdhane, Lilia, Boujemaa, Maroua, Dallali, Hamza, Sayeb, Marwa, Lahbib, Saida, Jaouadi, Hajer, Boudabbous, Hela, Zekri, Lotfi, Chargui, Mariem, Messaoud, Olfa, Elyounsi, Meriem, Kraoua, Ichraf, Zaouak, Anissa, Turki, Ilhem, Mokni, Mourad, Boucher, Sophie, Petit, Christine, Giraudet, Fabrice, Mbarek, Chiraz, Besbes, Ghazi, Halayem, Soumeyya, Zainine, Rim, Turki, Hamida, Tounsi, Amel, Bonnet, Crystel, Mrad, Ridha, Abdelhak, Sonia, Trabelsi, Mediha, Charfeddine, Cherine

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Identification of Eleven Novel BRCA Mutations in Tunisia: Impact on the Clinical Management of BRCA Related Cancers von Hamdi, Yosr, Mighri, Najah, Boujemaa, Maroua, Mejri, Nesrine, Ben Nasr, Sonia, Ben Rekaya, Mariem, Messaoud, Olfa, Bouaziz, Hanen, Berrazega, Yosra, Rachdi, Haifa, Jaidane, Olfa, Daoud, Nouha, Zribi, Aref, Ayari, Jihene, El Benna, Houda, Labidi, Soumaya, Ben Hassouna, Jamel, Haddaoui, Abderazzek, Rahal, Khaled, Benna, Farouk, Mrad, Ridha, Ben Ahmed, Slim, Boussen, Hamouda, Boubaker, Samir, Abdelhak, Sonia

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H syndrome: Clinical, histological and genetic investigation in Tunisian patients von Jaouadi, Hager, Zaouak, Anissa, Sellami, Khadija, Messaoud, Olfa, Chargui, Mariem, Hammami, Houda, Jones, Meriem, Jouini, Raja, Chadli Debbiche, Achraf, Chraiet, Karima, Fenniche, Sami, Mrad, Ridha, Mokni, Mourad, Turki, Hamida, Benkhalifa, Rym, Abdelhak, Sonia

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Lipid Profile Quantification and Species Discrimination of Pine Seeds through NIR Spectroscopy: A Feasibility Study von Khouja, Mariem, Páscoa, Ricardo N M J, Melo, Diana, Costa, Anabela S G, Nunes, M Antónia, Khaldi, Abdelhamid, Messaoud, Chokri, Oliveira, M Beatriz P P, Alves, Rita C

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An optimized protocol for in vitro propagation of Pyrus communis and Pyrus syriaca using apical-bud microcuttings von Mariem Lotfi, Chokri Bayoudh, Afifa Majdoub, Messaoud Mars

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High Frequency of Cardiovascular Complications in Tunisian Kawasaki Disease Patients: Need for a Further Awareness von Ben Chehida, Amel, Ben Messaoud, Sana, Ben Abdelaziz, Rim, Boudabous, Hela, Oujra, Mariem, Ben Turkia, Hadhami, Abdelmoula, Mohamed Slim, Azzouz, Hatem, Hakim, Kaothar, Tebib, Neji

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Molecular Characterization of Mycobacterium tuberculosis Strains Resistant to Isoniazid von Smaoui, S, Siala, M, Hadj Fredj, S, Kammoun, S, Marouane, C, Hachicha, S, Ghorbel, A, Gdoura, R, Slim, L, Ben Messaoud, T, Messadi, F

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Association between ACE polymorphism, cognitive phenotype and APOE E4 allele in a Tunisian population with Alzheimer disease von Achouri-Rassas, Afef, Ali, Nadia Ben, Cherif, Aroua, Fray, Saloua, Siala, Hajer, Zakraoui, Nouria Oudiaa, Hadj-Fredj, Sondes, Kechaou, Mariem, Anane, Nadia, Echebi, Slim, Messaoud, Taieb, Belal, Samir

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Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia von Sahli, Chaima Abdelhafidh, Bibi, Amina, Ouali, Faida, Fredj, Sondess Hadj, Dakhlaoui, Boutheina, Othmani, Rym, Laouini, Naouel, Jouini, Latifa, Ouenniche, Fekria, Siala, Hajer, Touhami, Imed, Becher, Mariem, Fattoum, Slaheddine, Toumi, Nour El Houda, Messaoud, Taieb

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c.1643_1644delTG XPC mutation is more frequent in Moroccan patients with xeroderma pigmentosum von Senhaji, Mohamed Amine, Abidi, Omar, Nadifi, Sellama, Benchikhi, Hakima, Khadir, Khadija, Ben Rekaya, Mariem, Eloualid, Abdelmajid, Messaoud, Olfa, Abdelhak, Sonia, Barakat, Abdelhamid

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Specific Aspects of Consanguinity: Some Examples from the Tunisian Population von Romdhane, Lilia, Halim, Nizar Ben, Rejeb, Insaf, Kefi, Rym, Bouyacoub, Yosra, Rekaya, Mariem Ben, Messai, Habib, Messaoud, Olfa, Riahi, Zied, Bonnet, Crystel, Rhouma, Faten Ben, Nagara, Majdi, Petit, Christine, McElreavey, Ken, Romeo, Giovanni, Abdelhak, Sonia

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Differential impact of consanguineous marriages on autosomal recessive diseases in Tunisia von Ben Halim, Nizar, Hsouna, Sana, Lasram, Khaled, Rejeb, Insaf, Walha, Asma, Talmoudi, Faten, Messai, Habib, Sabrine Ben Brick, Ahlem, Ouragini, Houyem, Cherif, Wafa, Nagara, Majdi, Rhouma, Faten Ben, Chouchene, Ibtissem, Ouechtati, Farah, Bouyacoub, Yosra, Ben Rekaya, Mariem, Messaoud, Olfa, Ben Ammar, Slim, El Matri, Leila, Tebib, Neji, Ben Dridi, Marie F., Mokni, Mourad, Amouri, Ahlem, Kefi, Rym, Abdelhak, Sonia

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A novel POLH gene mutation in a xeroderma pigmentosum-V Tunisian patient: phenotype–genotype correlation von REKAYA, MARIEM BEN, MESSAOUD, OLFA, MEBAZAA, AMEL, RIAHI, OLFA, AZAIEZ, HELA, KEFI, RIM, ZGHAL, MOHAMED, BOUBAKER, SAMIR, AMOURI, AHLEM, OSMAN-DHAHRI, AMEL BEN, ABDELHAK, SONIA, MOKNI, MOURAD

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