Dr. Nathan Fischel

 


Book Chapters

 

  1. Fischel-Ghodsian N: Anemia of iron deficiency and chronic disease. In: Gellis SS, and Kagan BM, Editors. Current Pediatric Therapy, 13th ed., p. 228-230, W.B. Saunders Co., Philadelphia, PA, 1990.

  2. Fischel-Ghodsian N: Prenatal diagnosis of hemoglobinopathies. In: Clinics in perinatology, Vol. 17, p. 811-828, W.B. Saunders Co., Philadelphia, PA, 1990.

  3. Shohat M, Fischel-Ghodsian N, Rotter JI, Danon YL: The gene for familial Mediterranean fever is mapped to 16p13.3-p13.1 with evidence for homogeneity. Advances in Mucosal Immunology. eds: J. Mestecky et. al., Plenum Press, New York, p. 901-903, 1995.

  4. Fischel-Ghodsian N, Falk RE: Hereditary Deafness. In: Rimoin DL, Connor JM, Pyeritz RE, and Emery AEH, Editors. Principles and Practice of Medical Genetics, 3rd ed., p. 1149-1170, Churchill Livingstone, Edinburgh, U.K., 1996.

  5. Fischel-Ghodsian N: Mitochondrially determined hearing impairment. In: Martini A, Stephens D, and Read AP, Editors. Genetics Hearing Impairment, p. 244-252, Whurr Publishers, London, U.K., 1996.

  6. Lotan R, Danon Y, Magal N, Ogur G, Tokguz G, Schwabe A, Fischel-Ghodsian N, Kastner D, Rotter JI, Schlezinger M, Shohat M: Frequencies of the various FMF core haplotypes in the MEFV locus. In: Sohar E, Gafni J, and Pras M, Editors. Familial Mediterranean Fever ,p. 104-108, Freund, London and Tel Aviv, 1997.

  7. Shohat M, Lotan R, Magal N, Ogur G, Tokguz G, Schwabe A, Fischel-Ghodsian N, Kastner D, Rotter JI, Schlezinger M, Danon Y: Association between ancestral haplotype in the MEFV locus and FMF-amyloidosis. In: Sohar E, Gafni J, and Pras M, Editors. Familial Mediterranean Fever ,p. 115-119, Freund, London and Tel Aviv, 1997.

  8. Fischel-Ghodsian N: Mitochondrial mutations and hearing loss. In: Lim D, Editor. Cell and Molecular Biology of the Ear, p. 133-142, Kluwer Academic / Plenum Publishers, New York, 2000.

  9. Fischel-Ghodsian N: Hearing loss and mitochondrial DNA mutations: Clinical implications and biological lessons. In: Keats B, Popper AN, Fay RR, Editors. Genetics and Auditory Disorders, p. 228-246, Springer Handbook of Auditory Research. Springer Verlag, New York, 2002.

  10. Fischel-Ghodsian N, Falk RE: Hereditary Deafness. In: Rimoin DL, Connor JM, Pyeritz RE, and Emery AEH, Editors. Principles and Practice of Medical Genetics, 4th ed., p. 3637-3672, Churchill Livingstone, Edinburgh, U.K., 2002.

  11. Falk RE, Fischel-Ghodsian N: Hereditary hearing loss. In: King RA, Rotter JI, and Motulsky AG, Editors. The Genetic Basis of Common Diseases, 2nd ed. p. 920-934, Oxford University Press, New York, 2003.

  12. Fischel-Ghodsian N: Genetic factors in aminoglycoside ototoxicity. In: Roland P, Rutka J, Editors. Ototoxicity, p. 144-152, BC Decker Inc Publisher, Hamilton, ON, Canada, 2004.

  13. Falk RE, Honrubia D, Fischel-Ghodsian N: Hereditary deafness. In: Rimoin DL, Connor JM, Pyeritz RE, and Korf BR, Editors. Principles and Practice of Medical Genetics, 5th ed., p. 3265-3302, Churchill Livingstone, Edinburgh, U.K., 2007.

 

 

Reviews

 

  1. Fischel-Ghodsian N: Mitochondrial genetics and hearing loss. New Developments in the Genetics of Hearing Impairment: Bulletin of the National Institute on Deafness and Other Communication Disorders Hereditary Hearing Impairment Resource Registry. Vol. 2, Number 2, p. 1-5, 1996.

  2. Fischel-Ghodsian N: Mitochondrial genetics and hearing loss - the missing link between genotype and phenotype. Proc Soc Exp Biol and Med 218, 1-6, 1998.

  3. Fischel-Ghodsian N: Genetic factors in aminoglycoside ototoxicity. Annals New York Acad Sci 884, 99-109, 1999.

  4. Fischel-Ghodsian N: Mitochondrial deafness mutations reviewed. Human Mutation 13, 261-270, 1999.

  5. Keithley EM, Linthicum F, and Fischel-Ghodsian N: Mitochondrial DNA, cytochrome oxidase and presbycusis. The Registry Volume 7, Number 1, 1999.

  6. Fischel-Ghodsian N: Mitochondrial Hearing Impairment. Audiological Med 1, 1-11, 2003.

  7. Fischel-Ghodsian N: Mitochondrial Deafness. Ear and Hearing 24, 303-313, 2003.

  8. Fischel-Ghodsian N, Kopke RD, Ge X: Mitochondrial dysfunction in hearing loss. Mitochondrion 4, 675-694, 2004.

  9. Fischel-Ghodsian N: Genetic factors in aminoglycoside ototoxicity. Pharmacogenomics 6, 27-36, 2005.

  10. Talaska AE, Schacht J, and Fischel-Ghodsian N: Mechanisms underlying aminoglycoside-induced hearing loss. Drug Discovery Today 3, 119-124, 2006.

 

 

Editorials

 

  1. Fischel-Ghodsian N: Mitochondrial mutations and hearing loss - paradigm for mitochondrial genetics. Am J Hum Genet 62, 15-19, 1998.

  2. Fischel-Ghodsian N: Mitochondrial DNA mutations and diabetes: Another step toward individualized Medicine. Ann Int Med 134, 777-779, 2001.

 

 

Other Publications

 

  1. Fischel N: The effects of partial and complete mechanical occlusion of the nasal passages on sleep structure and breathing in sleep. M.D. thesis, Technion School of Medicine, 1982.

  2. Fischel-Ghodsian N: Mitochondrial Diseases. N Engl J Med 349, 1293-1294, 2003 (letter).

 

 

Back to Dr. Fischel's Biography