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Galactosialidosis
Fast Urinary Screening of Oligosaccharidoses by MALDI-TOF/TOF Mass Spectrometry
4Th Glycoproteinoses International Conference Advances in Pathogenesis and Therapy
International Conference
The Lysosomal Sialic Acid Transporter Sialin Is Required for Normal CNS Myelination
Clinical, Biochemical, and Cytochemical Studies on a Japanese Salla Disease Case Associated with a Renal Disorder
I-Cell Disease): a Rare Condition Resembling Hurler Syndrome: a Case Report S Yang, TW Yeung, HY Lau Department of Radiology, Tuen Mun Hospital, Tuen Mun, Hong Kong
SSIEM Classification of Inborn Errors of Metabolism 2011
Collectively Common, Individually Rare Many
Lysosomal Storage Disorders: Urine Screening
Conventional and Unconventional Therapeutic Strategies for Sialidosis Type I
Lysosomal Storage Disorders Diagnostic Algorithm, Part 2
Novel Missense Mutations in the Human Lysosomal Sialidase Gene in Sialidosis Patients and Prediction of Structural Alterations of Mutant Enzymes
Emerging Trends in Transplantation of Inherited Metabolic Diseases
Lysosomal Storage Disorders Screen Interpretive Algorithm
Lysosomal Storage Disease Panel by Next-Generation Sequencing
In Ammatory Arthritis Complicating Galactosialidosis
Galactosialidosis
Lysosomal Storage Diseases, Diagnosis from Skin Lesions
Top View
Galactosialidosis.Pdf
The Genetic Nomenclature of Recessive Cerebellar Ataxias
Genes Associated with Neuraminidase-Deficiency Disorders (Sialidase/Gene Mapping/Complementation Analysis) 0
Metabolic Disorders (Children)
Early Infantile Galactosialidosis Presenting with an Unusual Renal
Glycoprotein Lysosomal Storage Disorders: K- and L-Mannosidosis, Fucosidosis and K-N-Acetylgalactosaminidase De¢Ciency
Genes Associated with Neuraminidase-Deficiency Disorders (Sialidase/Gene Mapping/Complementation Analysis) 0
Lysosomal Storage Diseases ª the Author(S) 2014 DOI: 10.1177/2326409813517663 Iem.Sagepub.Com
The Role of Hematopoietic Cell Transplant in the Glycoprotein Diseases
Metabolske Sykdommer V02
Diagnosis of Fucosidosis Through a Skin Rash
Insights Into the Diagnosis and Treatment of Lysosomal Storage Diseases
Physician's Guide to the Diagnosis, Treatment, and Follow-Up Of
Exploratory Investigation and Inherited Metabolic Diseases
Lysosomal Storage Diseases Carlos Ferreira George Washington University
2017 95-98 Galactosialidosis in a Newborn with A
Lysosomal Storage Diseases
Mouse Model for the Lysosomal Disorder Galactosialidosis and Correction of the Phenotype with Overexpressing Erythroid Precursor Cells
Gene Therapy for Lysosomal Storage Disorders with Neuropathology