Volume 94, Number 2 (2000), in the short analytical review “Animal Models of Myasthenia Gravis,” by Premkumar Christadoss, Mathilde Poussin, and Caishu Deng, pages 75–87 (doi:10.1006/clim.1999.4807)

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Clinical Immunology, Vol. 95, Iss. 2, 2000-05 ,pp. : 170-170

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Volume 26, Number 6 (2000), in the article “A New Exon 9 Glucose-6-phosphate Dehydrogenase Mutation (G6PD “Rehovot”) in a Jewish Ethiopian Family with Variable Phenotypes,” by Mona Iancovici-Kidon, Daliah Sthoeger, Ayala Abrahamov, Baruch Volach, Ernest Beutler, Terri Gelbart, and Yigal Barak, pages 567–571 (doi:10.1006/bcmd.2000.0334)

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Blood Cells, Molecules, and Diseases, Vol. 27, Iss. 1, 2001-01 ,pp. : 351-351

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Volume 25, Number 6 (1999), in the article “Analysis of Tlr4-Mediated LPS Signal Transduction in Macrophages by Mutational Modification of the Receptor,” by X. Du, A. Poltorak, M. Silva, and B. Beutler, pages 328–338 (doi:10.1006/bcmd.1999.0262)

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Blood Cells, Molecules, and Diseases, Vol. 26, Iss. 1, 2000-02 ,pp. : 9-9

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Volume 27, Number 2 (2001), in the article “Identification and Characterization of a Novel Mutation c.1090G>T (G325W) and Nine Common Mutant Alleles Leading to Gaucher Disease in Spanish Patients,” by M. A. Torralba, J. I. Pérez-Calvo, G. M. Pastores, A. Cenarro, P. Giraldo, and M. Pocoví, pages 489–495 (doi:10.1006/bcmd.2001.0410)

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Blood Cells, Molecules, and Diseases, Vol. 27, Iss. 3, 2001-03 ,pp. : 713-713

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Volume 28, Number 2 (2002), in the article “Low-Dose N-Butyldeoxynojirimycin (OGT 918) for Type I Gaucher Disease,” by Rene Heitner, Deborah Elstein, Johannes Aerts, Sonja van Weely, and Ari Zimran, pages 127–133 (doi:10.1006/bcmd.2002.0497)

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Blood Cells, Molecules, and Diseases, Vol. 28, Iss. 2, 2002-02 ,pp. : 301-301

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