Anatomy Bibliography

1. Bakker, E.; Breuning, M.H.; Ginjaar, H.B.; Helderman-van den Enden, A.T.J.M.; Tibben, A.; van den Bergen, J.C.; Vershuuren, J.J.G.M. “Duchenne/Becker muscular dystrophy in the family: have potential carriers been tested at a molecular level?” Journal of Clinical Genetics. Vol. 79 Issue 3, p236-242, 2011.

2. Chandramohan, Arthi; Lakshmi, Bremadesam Raman; Murugan, Sakthivel. “Use of multiplex ligation-dependent probe amplification (MLPA) for Duchenne musculardystrophy (DMD) gene mutation analysis” Indian Journal of Medical Research. Vol. 132 Issue 3, p303-311, 2010.

3. Bachrach, Estanislao; Bennett, Richard R.; Guyon, Jeffrey; Kunkel, Louis M.; Steffen, Leta. “Diagnosis and cell-based therapy for Duchenne muscular dystrophy in humans, mice, and zebrafish” Journal of Human Genetics. Vol. 51 Issue 5, p397- 406, 2006.

4. Awano, Hiroyuki; Matsuo, Masafumi; Nishio, Hisahide; Okizuka, Yo; Takeshima, Yasuhiro; Yagi, Mariko; Yamauchi, Yumiko; Zhang, Zhujun. “Mutation spectrum of the dystrophin gene in 442 Duchenne/Becker muscular dystrophy cases from one Japanese referral center” Journal of Human Genetics. Vol. 55 Issue 6, p379-388, 2010

5. Clark, Mary-Jo; Jih-Yuan Chen. “Family Resources and Parental Health in Families of Children With Duchenne MuscularDystrophy” Journal of Nursing Research. Vol. 18 Issue 4, p239-248, 2010.

6. Azeddoug, Houssine; Bellayou, Hanane; Hamzi, Khalil; Karkouri, Mehdil; Nadifi, Sellama; Rafai, Mohamed Abdou; Slassi, Ilham. “Duchenne and Becker Muscular Dystrophy: Contribution of a Molecular and Immunohistochemical Analysis in Diagnosis in Morocco” Journal of Biomedicine & Biotechnology. Regular Issue, p1-5, 2009.

7. Bouchet, Céline; Campbell, Kevin P.; Clarke, Nigel F.; Chouery, Eliane; Endo, Tamao; Gray, Françoise; Guicheney, Pascale; Manya, Hiroshi; Maugenre, Svetlana; Mégarbané, André; Peat, Rachel A.; Urtizberea, J. Andoni; Vandebrouck, Aurélie; Vuillaumier-Barrot, Sandrine; Willer, Tobias. “Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene” European Journal of Human Genetics. Vol. 19 Issue 4, p452-457, 2011.

8. Angelini, Corrado; Aurino, Stefania; Cacciottolo, Mafalda; Caserta, Imma Rosaria; Fanin, Marina; Minetti, Carlo; Nigro, Vincenzo; Numitone, Gelsomina; Piluso, Giulio; Politano, Luisa; Ricci, Enzo. “Congenital muscular dystrophy type 1D (MDC1D) due to a large intragenic insertion/deletion, involving intron 10 of the LARGE gene” European Journal of Human Genetics. Vol. 19 Issue 9, p974-980, 2011.

9. Kanagawa, Motoi; Toda, Tatsushi. “The genetic and molecular basis of muscular dystrophy: roles of cell–matrix linkage in the pathogenesis” Journal of Human Genetics. Vol. 51 Issue 11, p915-926, 2006.

10. Allen, David G.; Gervasio, Othon L.; Whitehead, Nicholas P.; Yeung, Ella W. “Calcium and the damage pathways in muscular dystrophy” Canadian Journal of Physiology & Pharmacology. Vol. 88 Issue 2, p83-91, 2010.

11. Davidson, Z. E.; Truby, H. “A review of nutrition in Duchenne muscular dystrophy” Journal of Human Nutrition & Dietetics. Vol. 22 Issue 5, p383-393, 2009.

12. Bower, Matthew; Brown, Charlotte A.; Ellis, Juliet A.; Felice, Kevin; Mendell, Jerry R.; Meriggioli, Matthew N.; Scharner, Juergen; Tarnopolsky, Mark; Zammit, Peter S. “Novel and recurrent EMD mutations in patients with Emery Dreifuss muscular dystrophy, identify exon 2 as a mutation hot spot” Journal of Human Genetics. Vol. 56 Issue 8, p589-594, 2011

13. Punnoose, Ann R. “Muscular Dystrophy” Journal of the American Medical Association. Vol. 306 Issue 22, p2526-2526, 2011

14. Aoyama, Chieko; Goto, Kanako; Hayashi, Yukiko K.; Ikeda, Kazutaka; Kale, Gulsev; Karahashi, Minako; Koksal, Burcu; Koumura, Tomoko; Kurihara, Mana; Mitsuhashi, Hiroaki; Mitsuhashi, Satomi; Noguchi, Satoru; Nonaka, Ikuya; Ohkuma, Aya; Quinlivan, Ros; Sewry, Caroline; Sher, Roger B.; Sugimoto, Hiroyuki; Taguchi, Ryo; Talim, Beril. “A Congenital Muscular Dystrophy with Mitochondrial Structural Abnormalities Caused by Defective De Novo Phosphatidylcholine Biosynthesis” American Journal of Human Genetics. Vol. 88 Issue 6, p845-851, 2011.

15. Awano, Hiroyuki; Itoh, Kyoko; Kumagai, Toshiyuki; Maruyama, Koichi; Matsuo, Masafumi; Okizuka, Yo; Takeshima, Yasuhiro; Yagi, Mariko; Zhang, Zhujun. “Low incidence of limb-girdle muscular dystrophy type 2C revealed by a mutation study in Japanese patients clinically diagnosed with DMD” BMC Medical Genetics. Vol. 11, p49-54, 2010.