Works matching DE "MAROTEAUX-Lamy syndrome"
Results: 29
Spinal Cord Compression in Maroteaux-Lamy Syndrome: Case Report and Review of the Literature with Effects of Enzyme Replacement Therapy.
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- Pediatric Neurosurgery, 2013, v. 48, n. 3, p. 191, doi. 10.1159/000345635
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- Publication type:
- Article
Non-sibling hematopoietic stem cell transplantation using myeloablative conditioning regimen in children with Maroteaux-Lamy syndrome: A brief report.
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- Pediatric Transplantation, 2017, v. 21, n. 5, p. n/a, doi. 10.1111/petr.12981
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- Article
Multiple Dentigerous Cysts as a Rare Presentation of Maroteaux-Lamy Syndrome.
- Published in:
- 2017
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- Publication type:
- Case Study
Roentgenographic diagnosis of mucopolysaccharidosis with particular reference to Morquio syndrome.
- Published in:
- 2012
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- Publication type:
- Case Study
A Rare Disease: Mucopolysaccharidosis Type 6 and Cardiac Involvement: Case Report.
- Published in:
- 2015
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- Publication type:
- Case Study
Recommendations for the management of MPS VI: systematic evidence- and consensus-based guidance.
- Published in:
- 2019
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- Publication type:
- journal article
Left clavicular fracture.
- Published in:
- 2016
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- Publication type:
- Editorial
Mucopolysaccharidosis IVA (Morquio A syndrome) and VI (Maroteaux-Lamy syndrome): under-recognized and challenging to diagnose.
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- Skeletal Radiology, 2014, v. 43, n. 3, p. 359, doi. 10.1007/s00256-013-1797-y
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- Publication type:
- Article
Mutational analysis of ARSB gene in mucopolysaccharidosis type VI: identification of three novel mutations in Iranian patients.
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- Iranian Journal of Basic Medical Sciences, 2018, v. 21, n. 9, p. 950, doi. 10.22038/IJBMS.2018.27742.6760
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- Article
Attenuated osteoarticular phenotype of type VI mucopolysaccharidosis: a report of four patients and a review of the literature.
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- Clinical Rheumatology, 2014, v. 33, n. 5, p. 725, doi. 10.1007/s10067-013-2423-z
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- Article
Another Novel Missense Mutation in ARSB Gene in Iran.
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- Acta Medica Iranica, 2017, v. 55, n. 9, p. 585
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- Article
Parents' experiences of living with, and caring for children, adolescents and young adults with Mucopolysaccharidosis (MPS).
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- Orphanet Journal of Rare Diseases, 2016, v. 11, p. 1, doi. 10.1186/s13023-016-0521-0
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- Article
Anaesthetic implications of the changing management of patients with mucopolysaccharidosis.
- Published in:
- 2016
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- Publication type:
- journal article
The phalangeal microgeodic syndrome in childhood: awareness leads to diagnosis.
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- European Journal of Pediatrics, 2013, v. 172, n. 6, p. 763, doi. 10.1007/s00431-013-1953-3
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- Publication type:
- Article
Diagnostic and treatment strategies in mucopolysaccharidosis VI.
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- Application of Clinical Genetics, 2015, v. 8, p. 245, doi. 10.2147/TACG.S68650
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- Publication type:
- Article
Dose Responsive Effects of Subcutaneous Pentosan Polysulfate Injection in Mucopolysaccharidosis Type VI Rats and Comparison to Oral Treatment.
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- PLoS ONE, 2014, v. 9, n. 6, p. 1, doi. 10.1371/journal.pone.0100882
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- Publication type:
- Article
Illness Perception and Clinical Treatment Experiences in Patients with M. Maroteaux-Lamy (Mucopolysaccharidosis Type VI) and a Turkish Migration Background in Germany.
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- PLoS ONE, 2013, v. 8, n. 6, p. 1, doi. 10.1371/journal.pone.0066804
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- Publication type:
- Article
ANESTHESIA MANAGEMENT IN A PATIENT WITH MAROTEAUX-LAMY SYNDROME.
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- Nobel Medicus Journal, 2012, v. 8, n. 1, p. 114
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- Publication type:
- Article
Evaluation of spinal involvement in children with mucopolysaccharidosis VI: the role of MRI.
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- British Journal of Radiology, 2018, v. 91, n. 1085, p. N.PAG, doi. 10.1259/bjr.20170744
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- Article
Mucopolysaccharidosis type VI in a juvenile miniature schnauzer dog with concurrent hypertriglyceridemia, necrotizing pancreatitis, and diabetic ketoacidosis.
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- 2015
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- Publication type:
- Case Study
Diffuse dermal melanocytosis in two patients with Sandhoff disease and mucopolysaccharidosis VI.
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- International Journal of Dermatology, 2014, v. 53, n. 6, p. 736, doi. 10.1111/ijd.12303
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- Article
DIAGNOSTYKA I POSTĘPOWANIE TERAPEUTYCZNE U DZIECI Z MUKOPOLISACHARYDOZĄ TYPU VI.
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- Przeglad Pediatryczny, 2012, v. 42, n. 3, p. 149
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- Publication type:
- Article
Mucopolysaccharidosis VI in cats – clarification regarding genetic testing.
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- BMC Veterinary Research, 2016, v. 12, p. 1, doi. 10.1186/s12917-016-0764-y
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- Publication type:
- Article
IgE-Mediated Hypersensitivity and Desensitisation with Recombinant Enzymes in Pompe Disease and Type I and Type VI Mucopolysaccharidosis.
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- International Archives of Allergy & Immunology, 2016, v. 169, n. 3, p. 198, doi. 10.1159/000446154
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- Publication type:
- Article
Evaluation of oral manifestations of patients with mucopolysaccharidosis IV and VI: clinical and imaging study.
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- Clinical Oral Investigations, 2018, v. 22, n. 1, p. 201, doi. 10.1007/s00784-017-2100-8
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- Publication type:
- Article
Hemifacial Spasm in Mucopolysaccharidosis Type VI (Maroteaux-Lamy Syndrome).
- Published in:
- 2018
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- Publication type:
- Case Study
Bilateral nonsyndromic dentigerous cyst in a 10-year-old child: A case report and literature review.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
Haploidentical stem cell transplantation in two children with mucopolysaccharidosis VI: clinical and biochemical outcome.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-134
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- Publication type:
- Article
Mucopolysaccharidosis type VI phenotypes-genotypes and antibody response to galsulfase.
- Published in:
- Orphanet Journal of Rare Diseases, 2013, v. 8, n. 1, p. 1, doi. 10.1186/1750-1172-8-51
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- Publication type:
- Article