Diagnosis of Attenuated Mucopolysaccharidosis VI: Clinical, Biochemical, and Genetic Pitfalls

Pediatrics - United States
doi 10.1542/peds.2018-0658
Full Text
Abstract

Available in full text

Date
Authors
Publisher

American Academy of Pediatrics (AAP)

Related search

Mucopolysaccharidosis VI Pathophysiology Diagnosis and Treatment

Frontiers in Bioscience - Landmark
ImmunologyMolecular BiologyBiochemistryMicrobiology MedicineGenetics
2017English

Attenuated Form of Type II Mucopolysaccharidoses (Hunter Syndrome): Pitfalls and Potential Clues in Diagnosis

BMJ Case Reports
Medicine
2018English

Clinical Hints to Diagnosis of Attenuated Forms of Mucopolysaccharidoses

Italian Journal of Pediatrics
Child HealthPediatricsPerinatology
2018English

Analysis of Mucopolysaccharidosis Type VI Through Integrative Functional Metabolomics

International Journal of Molecular Sciences
Organic ChemistryMolecular BiologyTheoretical ChemistryInorganic ChemistryComputer Science ApplicationsSpectroscopyMedicineCatalysisPhysical
2019English

Allogeneic CD34 Selected Peripheral Stem Cell Transplant for Maroteaux–Lamy Syndrome (Mucopolysaccharidosis Type VI): Rapid Haemopoietic and Biochemical Reconstitution

Bone Marrow Transplantation
TransplantationHematology
1998English

Lactose Intolerance: Diagnosis, Genetic, and Clinical Factors

Clinical and Experimental Gastroenterology
Gastroenterology
2012English

Genetic Diagnosis and Testing in Clinical Practice

Clinical Medicine and Research
MedicineHome CareCommunity
2006English

Clinical and Technical Aspects of Preimplantation Genetic Diagnosis

Expert Review of Obstetrics & Gynecology
2008English

Diagnosis and Management of Ophthalmological Features in Patients With Mucopolysaccharidosis

British Journal of Ophthalmology
Molecular NeuroscienceOphthalmologySensory SystemsCellular
2010English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy