How to Cite this Article: Karimzadeh P. Fabery Disease (A kind of Lysosomal Storage Disease). Iran J Child Neurol Autumn 2012; 6:4(suppl. 1):6. Pls See PDF
Fabry disease is an X-linked inherited lysosomal disorder due to dysfunctions of the lysosomal enzym...
How to Cite This Article: Houshmand M. Genetic investigation of Lukodystrophy in Iran. Iran J Child ...
Fabrys disease is a lysosomal storage disorder, caused due to mutation in the GLA gene in X-chromoso...
How to Cite this Article: Houshmand M, Tonekaboni SH, Karimzadeh P, Aryani O, AshrafiMR, Salehpour S...
How to Cite this Article: Zamani Gh. Approach to Lysosomal Disorders. Iran J Child Neurol Autumn 201...
How to Cite this Article: Ghofrani M. Lysosomal Storage Disease (LSDs). Iran J Child Neurol. 2015 Au...
How to Cite this Article: Alaei F. Cardiac Involvement in Lysosomal Diseases. Iran J Child Neurol Au...
How to Cite this Article: Taghdiri MM. Type 2 Gaucher Disease (Acute Infantile Gaucher Disease or Ne...
How to Cite This Article: Zamani Gh.R. Neuroimaging Findings in Storages Disease of Children. Iran J...
How to Cite this Article: Shakiba M. Diagnosis in Lysosomal Disorders. Iran J Child Neurol Autumn 20...
How to Cite this Article: Nilipour Y. Lysosomal Myopathies. Iran J Child Neurol Autumn 2012; 6:4 (su...
How to Cite this Article: Ashrafi MR, Tavasoli AR. Infantile-Onset Pompe Disease. Iran J Child Neu...
How to Cite This Article: Ahmadabadi F. Neurometabolic Registry Site in Iran (Leukodystrophies). Ira...
Fabry disease is an X-linked recessive lysosomal storage disorder caused by a deficiency of α-galact...
Fabry disease is one of the lysosomal storage disorders, that results from progressive multiorgan a...
Fabry disease is an X-linked inherited lysosomal disorder due to dysfunctions of the lysosomal enzym...
How to Cite This Article: Houshmand M. Genetic investigation of Lukodystrophy in Iran. Iran J Child ...
Fabrys disease is a lysosomal storage disorder, caused due to mutation in the GLA gene in X-chromoso...
How to Cite this Article: Houshmand M, Tonekaboni SH, Karimzadeh P, Aryani O, AshrafiMR, Salehpour S...
How to Cite this Article: Zamani Gh. Approach to Lysosomal Disorders. Iran J Child Neurol Autumn 201...
How to Cite this Article: Ghofrani M. Lysosomal Storage Disease (LSDs). Iran J Child Neurol. 2015 Au...
How to Cite this Article: Alaei F. Cardiac Involvement in Lysosomal Diseases. Iran J Child Neurol Au...
How to Cite this Article: Taghdiri MM. Type 2 Gaucher Disease (Acute Infantile Gaucher Disease or Ne...
How to Cite This Article: Zamani Gh.R. Neuroimaging Findings in Storages Disease of Children. Iran J...
How to Cite this Article: Shakiba M. Diagnosis in Lysosomal Disorders. Iran J Child Neurol Autumn 20...
How to Cite this Article: Nilipour Y. Lysosomal Myopathies. Iran J Child Neurol Autumn 2012; 6:4 (su...
How to Cite this Article: Ashrafi MR, Tavasoli AR. Infantile-Onset Pompe Disease. Iran J Child Neu...
How to Cite This Article: Ahmadabadi F. Neurometabolic Registry Site in Iran (Leukodystrophies). Ira...
Fabry disease is an X-linked recessive lysosomal storage disorder caused by a deficiency of α-galact...
Fabry disease is one of the lysosomal storage disorders, that results from progressive multiorgan a...
Fabry disease is an X-linked inherited lysosomal disorder due to dysfunctions of the lysosomal enzym...
How to Cite This Article: Houshmand M. Genetic investigation of Lukodystrophy in Iran. Iran J Child ...
Fabrys disease is a lysosomal storage disorder, caused due to mutation in the GLA gene in X-chromoso...
DOI