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Reisch AS, Elpeleg O. (2007) Enzymatic assays of TCA and PDHc. In mitochondria 2nd Ed , Eds Pon and Schon E.Academic Press USA. Methods in Cell Biology 80:199-222
Saada (Reisch) A.(2012). Complex subunits and assembly genes: Complex I. p185-202. In Mitochondrial disorders caused by nuclear genes. Ed:Wong L.J. Springer-Verlag
Chowers Y, Kerrison JB, Saada API. (2013). Mitochondrial and peroxisomal disorders. p227-239. In Pediatric retina 2nd ed. Eds: Harnett M.E, Capone T, Caputo G, Keats B, Trese M. Wolters Kluwer/LipcottWilliams & Wilkins.
Soiferman D, Saada A.(2014) The use of fibroblasts from patients with inherited mitochondrial disorders for pathomechanistic studies and evaluation of therapies. In The functions, disease-related dysfunctions, and therapeutic targeting of neuronal mitochondria .p 378-393 Eds: Gribkoff VK, Jonas EA. John Wiley & Sons Inc.
Edvardson SC, Saada (Reisch)API (2014) Complex II Deficiency – Leukoencephalopathy due to mutated SDHAF1.In.Mitochondrial Case Studies: Underlying Mechanisms and Diagnosis. Eds.Saneto RP,Parikh S, CohenBH. Academic Press/Elsevier p.265-271
Khateb, Saada A, Yu-Wai-Man P,Kerrison JB Chowers I (2020). Mitochondrial and Peroxisomal Disorders In Pediatric retina 3nd ed. Eds: Harnett M.E, Capone T, Caputo G, Keats B, Trese M. Wolters Kluwer/LipcottWilliams & Wilkins in press
Bennet MJ, Sheng F, Saada A. (2020) Biochemical assays of TCA cycle and β-oxidation metabolites. In In mitochondria 3rd Ed , Methods in Cell Biology Volume 155 , Eds Pon and Schon E. Elsevier in press
