A novel mutation of IL1RN in the deficiency of interleukin‐1 receptor antagonist syndrome: Description of two unrelated cases from Brazil von Jesus, Adriana A., Osman, Mazen, Silva, Clovis A., Kim, Peter W., Pham, Tuyet‐Hang, Gadina, Massimo, Yang, Barbara, Bertola, Débora R., Carneiro‐Sampaio, Magda, Ferguson, Polly J., Renshaw, Blair R., Schooley, Ken, Brown, Michael, Al‐Dosari, Asma, Al‐Alami, Jamil, Sims, John E., Goldbach‐Mansky, Raphaela, El‐Shanti, Hatem

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Enhancing photodynamic therapy efficacy through silica nanoparticle-mediated delivery of temoporfin for targeted in vitro breast cancer treatment von Makhadmeh, Ghaseb N., AlZoubi, Tariq, Aljarrah, Amer M., abu mhareb, Mohammad hasan, Alami, Jamil H.Al, Zyoud, Samer H.

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Biallelic SCN10A mutations in neuromuscular disease and epileptic encephalopathy von Kambouris, Marios, Thevenon, Julien, Soldatos, Ariane, Cox, Allison, Stephen, Joshi, Ben‐Omran, Tawfeg, Al‐Sarraj, Yasser, Boulos, Hala, Bone, William, Mullikin, James C., Masurel‐Paulet, Alice, St‐Onge, Judith, Dufford, Yannis, Chantegret, Corrine, Thauvin‐Robinet, Christel, Al‐Alami, Jamil, Faivre, Laurence, Riviere, Jean Baptiste, Gahl, William A., Bassuk, Alexander G., Malicdan, May Christine V., El‐Shanti, Hatem

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Mutations in the CCN gene family member WISP3 cause progressive pseudorheumatoid dysplasia von Hul, Els Van, Warman, Matthew L, Al-Alami, Jamil, Roudier, Jean, Bahabri, Sultan A, Hurvitz, Jennifer R, Pauli, Richard M, El-Shanti, Hatem, Rezai-Delui, Hossien, Van Hul, Wim, Suwairi, Wafaa M, Legius, Eric, Holderbaum, Daniel, Herd, J. Kenneth, Superti-Furga, Andrea, Le Merrer, Martine

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Exploration of laser-assisted chemical bath for enhancing synthesis of undoped and nickel-doped zinc oxide and its potential applications in water purification and mitigating antim... von Zyoud, Samer H., Alalalmeh, Samer O., Hegazi, Omar E., Alami, Jamil H., Abdullah, Che Azurahanim Che, Yahia, I.S., Hassan, Nageeb, Ashames, Akram, Zahran, H.Y., Bloukh, Samir Haj, Shahwan, Moyad, Zyoud, Ahed H., Jairoun, Ammar Abdulrahman, Qamhieh, Naser

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Familial mediterranean fever mutation frequencies and carrier rates among a mixed Arabic population von AL-ALAMI, Jamil R, TAYEH, Marwan K, NAJIB, Dana A, ABU-RUBAIHA, Zaid A, MAJEED, Hassan A, EL-KHATEEB, Mohammad S, EL-SHANTI, Hatem I

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Biallelic SCN 10A mutations in neuromuscular disease and epileptic encephalopathy von Kambouris, Marios, Thevenon, Julien, Soldatos, Ariane, Cox, Allison, Stephen, Joshi, Ben‐Omran, Tawfeg, Al‐Sarraj, Yasser, Boulos, Hala, Bone, William, Mullikin, James C., Masurel‐Paulet, Alice, St‐Onge, Judith, Dufford, Yannis, Chantegret, Corrine, Thauvin‐Robinet, Christel, Al‐Alami, Jamil, Faivre, Laurence, Riviere, Jean Baptiste, Gahl, William A., Bassuk, Alexander G., Malicdan, May Christine V., El‐Shanti, Hatem

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Zinc in normal and pathological human prostate gland von BATAINEH, Ziad M, BANI HANI, Ibrahim H, AL-ALAMI, Jamil R

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Nuclear zinc in liver of cadmium and zinc treated rats von Bataineh, Ziad M, Al-Alami, Jamil R

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Homozygous AMN mutation in hereditary selective intestinal malabsorption of vitamin B12 in Jordan von AL-ALAMI, Jamil R, TANNER, Stephan M, TAYEH, Marwan K, DE LA CHAPELLE, Albert, EL-SHANTI, Hatem

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Linkage analysis of a large inbred family with congenital megaloblastic anemia von AL-ALAMI, Jamil R, TAYEH, Marwan K, AL-SHEYYAB, Mahmoud Y, EL-SHANTI, Hatem I

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Reactivation of latent Toxoplasma gondii in immunocompromised cancer patients von Khabaz, Mohamad Nidal, Elkhateeb, Layla, Al-Alami, Jamil

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The identification of CNVs in patients and their association with diseases and phenotypes von Alami, Jamil

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Serum sex hormones in premenopausal women with coronary heart disease von Mohamad, Mohamad Jaffer, Karayyem, Mohamad, Mohammad, Mukhallad A, Al-Alami, Jamil, Al-Hader, Adulfatah

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Golgi-type I and Golgi-type II Neurons in the Ventral Anterior Thalamic Nucleus of the Adult Human: Morphological Features and Quantitative Analysis von Al-Hussain (Bani Hani), Saleh M., El-Dwairi, Qasim A., Bataineh, Ziad M., Al-Haidari, Mohammad S., Al-Alami, Jamil

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Bcl-2 gene rearrangement in Jordanian follicular and diffuse large B-cell lymphomas von ALMASRI, Nidal M, AL-ALAMI, Jamil, FAZA, Mohammad

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The pattern of peripheral blood chromosomal abnormalities in Northern Jordan von EL-SHANTI, Hatem, AL-ALAMI, Jamil

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Atypical Rett syndrome diagnosis by molecular testing von Vasiliki, Chini, Elsayed, Zakaria, Alami, Jamil

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Assignment of gene responsible for progressive pseudorheumatoid dysplasia to chromosome 6 and examination of COL10A1 as candidate gene von el-Shanti, H, Murray, J C, Semina, E V, Beutow, K H, Scherpbier, T, al-Alami, J

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The Assignment of the Gene Responsible for Congenital Cataract and Micropthalmia to the Pericentromeric Region of the X Chromosome and Examination of Candidate Genes von Chini, Vasiliki

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