|
1.
|
Approach to Lysosomal Disorders ZAMANI, Gholamreza; Associate Professor of Pediatric Neurology, Children’s Medical Center, Tehran University of Medical Sciences (TUMS ), Tehran, Iran
|
|
2.
|
Lysosomal Myopathies NILIPOUR, Yalda; 1. Neuropathologist, Shahid Beheshti University of Medical Sciences, Tehran, Iran
|
|
3.
|
Cardiac Involvement in Lysosomal Diseases ALAEI, Fariba; 1.Assistant Professor of Pediatric Cardiology, Mofid Children’s Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
|
|
4.
|
Mucopolysaccharidosis Type 1 ALAEE, Mohammad Reza; Associate Professor of Endocrinology, Mofid Children Hospital,Shahid Beheshti University of Medical Sciences (SBMU), Tehran, Iran
|
|
5.
|
Electrodiagnostic Studies, “Role in The Diagnosis And Follow-Up in Children With Pompe Disease” MOHAMMADI, Mahmoud; 1.Professor of Pediatric Neurology, Children’s Medical Center, Tehran University of Medical Sciences, Tehran, Iran
|
|
6.
|
Rheumatologic Manifestations of Lysosomal Storage Diseases SHIARI, Reza; 1.Associate Professor of Pediatric Rheumatology, Shahid Beheshti University of Medical Sciences, Mofid Children’s Hospital, Tehran-Iran - JAVADI PARVANEH, Vadood; 2. Fellow of Pediatric Rheumatology, Shahid Beheshti University of Medical Sciences, Mofid Children’s Hospital, Tehran-Iran
|
|
7.
|
Fabry Disease (A Kind of Lysosomal Storage Disease) KARIMZADEH, Parvaneh
|
|
8.
|
Seizure is a rare presentation for acute hemolysis due to G6PD deficiency. We report a previously healthy boy who presented initially with seizure and cyanosis and subsequently acute hemolysis, due to glucose-6-phosphate dehydrogenase deficiency (G6PD) an FAYYAZI, Afshin; Pediatric Neurologist, Hamedan University of Medical Sciences, Hamedan, Iran - KHAJEH, Ali; Pediatric Neurologist, Zahedan University of Medical Sciences, Zahedan, Iran - ESFAHANI, Hosein; Pediatric Hematologist, Hamedan University of Medical Sciences, Hamedan, Iran
|
|
9.
|
Type 2 Gaucher Disease (Acute Infantile Gaucher Disease or Neuropathic Type) TAGHDIRI, Mohammad Mehdi; 1. Associate Professor of Pediatric Neurology, Pediatric Neurology Research Center, Shahid Beheshti University of Medical Sciences, Tehran, Iran 2. Associate Professor of Pediatric Neurology, Department of Pediatric Neurology, Mofid Children Hospital, Shahid Beheshti University of Medical Sciences, Tehran, Iran
|
|
10.
|
Lysosomal Storage Disease in Iran (Report of Molecular Study) HOUSHMAND, Massoud; 1. Assistant Professor of Human Molecular Genetics, Department of Medical Genetic, National Institute for Genetic Engineering and Biotechnology, Tehran, Iran - TONEKABONI, Seyed Hassan; 2.Professor of Pediatric Neurology, Pediatric Neurology Research Center, Shahid Beheshti University of Medical sciences,Tehran, Iran - KARIMZADEH, Parvaneh; Professor of Pediatric Neurology, Pediatric Neurology Research Center, Shahid Beheshti University of Medical sciences,Tehran, Iran - ARYANi, Omid; Genetic Counselor, Medical Genetic Dep. Special Medical Center, Tehran, Iran - ASHRAFI, Mahmoudreza; Professor of Pediatric Neurology, Growth and Development Research Center, Children´s Medical Center, Tehran University of Medical Science, Tehran, Iran - SALEHPOUR, Shadab; Associate Professor of Pediatric Endocrinology and Metabolism, Shahid Beheshti University of Medical Sciences, Tehran, Iran - BADV, Shervin; Assistant Professor of Pediatric Neurology, Zanjan University of Medical Sciences, Zanjan, Iran - SHAKIBA, Marjan; Associate Professor of Pediatric Endocrinology and Metabolism, Shahid Beheshti University of Medical Sciences, Tehran, Iran - ALAEE, Mohammad Reza; Associate Professor of Endocrinology, Shahid Beheshti University of Medical Sciences (SBMU), Tehran, Iran - FARSHIDI, Shahla; Nasle Omid Hope Foundation
|
