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Sankar Surendran and Vykuntaraju K. Gowda
322
[55] Bennet, MJ; Gibson, KM; Sherwood, WG; Divry, P; Rolland, MO;
Elpeleg, ON; Rinaldo, P; Jakobs, C. Reliable prenatal diagnosis of
Canavan disease (aspartoacylase deficiency): comparison of
enzymatic and metabolite analysis. J. Inherit. Metab. Dis. 1993, 16,
831–836.
[56] Kelley, RI. Prenatal detection of canavan disease by measurement of
N-acetyl-L-aspartate in amniotic fluid. J. Inherit. Metab. Dis. 1993,
16, 918–919.
[57] Al-Dirbashi, OY; Kurdi, W; Imtiaz, F; Ahmad, AM; Al-Sayed, M;
Tulbah, M; Al-Nemer, M; Rashed, MS. Reliable prenatal diagnosis
of Canavan disease by measuring N-acetylaspartate in amniotic fluid
using liquid chromatography tandem mass spectrometry. Prenat.
Diagn. 2009, 29, 477–480.
[58] Yaron, Y; Schwartz, T; Mey-Raz, N; Amit, A; Lessing, JB; Malcov,
M. Preimplantation genetic diagnosis of Canavan disease. Fetal.
Diagn. Ther. 2005, 20, 465-468.
[59] Segel, R; Anikster, Y; Zevin, S; Steinberg, A; Gahl, WA; Fisher, D;
Staretz-Chacham, O; Zimran, A; Altarescu, G. A safety trial of high
dose glyceryl triacetate for Canavan disease. Mol. Genet. Metab.
2011,103, 203-206.
[60] Madhavarao, CN; Arun, P; Anikster, Y; Mog, SR; Staretz-Chacham,
O; Moffett, JR; Grunberg, NE; Gahl, WA, Namboodiri, AMA.
Glyceryl triacetate for Canavan disease: A low-dose trial in infants
and evaluation of a higher dose for toxicity in the tremor rat model.
J. Inherit. Metab. Dis. 2009, 32, 640-650.
[61] Hull, V; Wang, Y; Burns, T; Zhang, S; Sternbach, SJ; Guo, F;
Pleasure, D. Antisense oligonucleotide reverses leukodystrophy in
Canavan disease mice. Ann. Neurol. 2020, 87, 480-485.
[62] Baslow, M; Kitada, K; Suckow, RF; Hungund, BL; Serikawa, T. The
effects of lithium chloride and other substances on levels of brain
NAA in Canavan disease-like rats. Neurochem. Res. 2002, 27, 403–
406.
[63] Bannerman, P; Guo, F; Chechneva, O; Burns, T; Zhu, X; Wang, Y;
Kim, B; Singhal, NK; McDonough, JA; Pleasure, D. Brain Nat 8l
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Current Trends in Canavan Disease Research …
323
knockdown suppresses spongiform leukodystrophy in an
aspartoacylase-deficient Canavan Disease mouse model. Mol. Ther.
2018, 26, 793-800.
[64] Gessler, DJ; Li, D; Xu, H; Su, Q; Sanmiguel, J; Tuncer, S; Moore, C;
King, J; Matalon, R; Gao, G. Redirecting N-acetylaspartate
metabolism in the central nervous system normalizes myelination and
rescues Canavan disease. JCI. Insight. 2017, 2, e90807.
[65] Maier, H; Wang-Eckhardt, L; Hartmann, D; Gieselmann, V;
Eckhardt, M. N-Acetylaspartate synthase deficiency corrects the
myelin phenotype in a Canavan Disease mouse model but does not
affect survival time. J. Neurosci. 2015, 35, 14501-14516.
[66] Appu AP; Moffett, JR; Arun, P; Moran, S; Nambiar, V; Krishnan,
JKS; Puthillathu, P; Namboodiri AMA. Increasing N-acetylaspartate
in the Brain during Postnatal Myelination Does Not Cause the CNS
Pathologies of Canavan Disease. Front. Mol. Neurosci. 2017, 10,
161.
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ABOUT THE EDITOR
Sankar Surendran
College Station, Texas 77845, USA
Email: ssanka12@gmail.com
Education: MS, PhD
Awards and Honors: 6
Membership in Professional Societies: 13
Publications: https://www.researchgate.net/profile/Sankar_Surendran
Original Articles: 44
Abstracts: 12
Review Articles: 18
Book Chapters: 8
Books:
1) Neurochemistry of metabolic Diseases: lysosomal storage
diseases, phenylketonuria and Canavan disease (2007) (Editor:
Sankar Surendran) Transworld research network, INDIA
2) Neurochemistry of metabolic Diseases: lysosomal storage
diseases, phenylketonuria and Canavan disease (ebook-2011)
(hard copy-2013) (Editor: Sankar Surendran) NOVA publishers
Inc, USA
Presentation of Work in National/International Meetings: 14
Attending Seminars, Symposia, Courses and Workshops: 21
International Examiner PhD Thesis: 8
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LIST OF CONTRIBUTORS
Dr. Fatma Al-Jasmi, MBBS
Department of Genetics & Genomics and Department of Paediatrics,
College of Medicine and Health Sciences, United Arab Emirates
University, Al Ain, United Arab Emirates; Department of Paediatrics,
Tawam Hospital, Al Ain, United Arab Emirates
Aisha Al-Shamsi, MBBS
Department of Paediatrics, Tawam Hospital, Al Ain, United Arab Emirates
Dr. Amal Al Tenaiji, MBBS
Department of Paediatrics, Sheikh Khalifa Medical Centre Hospital,
Abu Dhabi, United Arab Emirates
Dr. Fatma Al-Yahyai, MBBS
Department of Paediatrics, Tawam Hospital, Al Ain, United Arab Emirates
Dr. Bassam R. Ali, PhD
Department of Genetics & Genomics, Department of Pathology,
College of Medicine and Health Sciences, United Arab Emirates
University, Al Ain, United Arab Emirates
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List of Contributors
328
Dr. Mahmoud R. Ashrafi, MD
Myelin Disorders Clinic, Pediatric Neurology Division,
Children's Medical Center, Pediatrics Center of Excellence,
Tehran University of Medical Sciences, Tehran, Iran
Joanna Brokowska, MS
Department of Molecular Biology, University of Gdansk,
Wita Stwosza 59, 80-308 Gdansk, Poland
Dr. Jaume Campistol, MD, PhD
PKU Unit, Department of Pediatric Neurology, Hospital Sant Joan de Deu,
Barcelona. Spain
Dr. Soumya V. Chandrasekharan, MD
Department of Neurology, Sree Chitra Tirunal Institute for
Medical Sciences and Technology, Trivandrum, India
Zuzanna Cyske, MS
Department of Molecular Biology, University of Gdansk,
Wita Stwosza 59, 80-308 Gdansk, Poland
Lidia Gaffke, MS
Department of Molecular Biology, University of Gdansk,
Wita Stwosza 59, 80-308 Gdansk, Poland
Dr. Masoud Garshasbi, PhD
Department of Medical Genetics, Faculty of Medical Sciences,
Tarbiat Modares University, Tehran, Iran
Dr. Vykuntaraju K. Gowda, DCH, DNB, DM
Department of Pediatric Neurology, Indira Gandhi Institute
of Child Health, Bangalore, India and Child Neurology and
Rehabilitation Center, Bangalore, India
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List of Contributors
329
Dr. Morteza Heidari, MD
Myelin Disorders Clinic, Pediatric Neurology Division,
Children's Medical Center, Pediatrics Center of Excellence,
Tehran University of Medical Sciences, Tehran, Iran
Dr. Jozef Hertecant, MD
Department of Paediatrics, College of Medicine and Health Sciences,
United Arab Emirates University, Al Ain, United Arab Emirates;
Department of Paediatrics, Tawam Hospital, Al Ain, United Arab Emirates
Dr. Ali Hosseini, PhD
Prenatal Diagnosis and Genetic Research Center, Dastgheib Hospital,
Shiraz University of Medical Sciences, Shiraz, Iran
Dr. Fedah E. Mohamed, PhD
Department of Genetics & Genomics and Department of Pathology,
College of Medicine and Health Sciences,
United Arab Emirates University, Al Ain, United Arab Emirates
Dr. Adriana M. Montano, PhD
Department of Pediatrics and Department of Biochemistry and
Molecular Biology, School of Medicine, Saint Louis University,
St. Louis, Missouri, USA
Aadhira Nair, MS
Foundation for Research in Genetics and Endocrinology,
Institute of Human Genetics, Ahmedabad, Gujarat, India
Dr. Sruthi S. Nair, DM
Department of Neurology, Sree Chitra Tirunal Institute for
Medical Sciences and Technology, Trivandrum, India
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List of Contributors
330
Dr. Karolina Pierzynowska, PhD
Department of Molecular Biology, University of Gdansk,
Wita Stwosza 59, 80-308 Gdansk, Poland
Dr. Magdalena Podlacha, PhD
Department of Molecular Biology, University of Gdansk,
Wita Stwosza 59, 80-308 Gdansk, Poland
Dr. Srinivasagam Rajasankar MS, PhD
Velammal Medical College Hospital & Research Institute,
Tamil Nadu, India
Estera Rintz, MS
Department of Molecular Biology, University of Gdansk,
Wita Stwosza 59, 80-308 Gdansk, Poland
Dr. Parastoo Rostami, MD
Growth and Development Research Center,
Division of Endocrinology and Metabolism, Children’s Medical Center,
Tehran University of Medical Sciences, Tehran, Iran
Dr. Consolato Sergi MD, PhD, MPH, FRCPC, FCAP, FACSc,
Department of Laboratory Medicine and Pathology, University of Alberta,
Edmonton, AB, Canada
Dr. Jayesh Sheth, PhD, FICMCH
Foundation for Research in Genetics and Endocrinology,
Institute of Human Genetics, Ahmedabad, Gujarat, India
Dr. Soumya Sundaram, DM
Department of Neurology, Sree Chitra Tirunal Institute for
Medical Sciences and Technology, Trivandrum, Kerala, India
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List of Contributors
331
Dr. Ali R. Tavasoli, MD
Myelin Disorders Clinic, Pediatric Neurology Division,
Children's Medical Center; Pediatrics Center of Excellence,
Tehran University of Medical Sciences, Tehran, Iran
Dr. Veerappachetty Venkateshgobi, BHMS, MS, PhD
Department of Anatomy, Sivaraj Medical Colleges, Tamil Nadu, India
Dr. Grzegorz Wegrzyn, MS, PhD, DSc
Department of Molecular Biology, University of Gdańsk,
Wita Stwosza 59, 80-308, Gdansk, Poland
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