Cargando…

Correction: Disease and patient characteristics in NP-C patients: findings from an international disease registry

Detalles Bibliográficos
Autores principales:	Patterson, Marc C, Mengel, Eugen, Wijburg, Frits A, Muller, Audrey, Schwierin, Barbara, Drevon, Harir, Vanier, Marie T, Pineda, Mercé
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	BioMed Central 2013
Materias:	Correction
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3655891/ http://dx.doi.org/10.1186/1750-1172-8-73

Ejemplares similares

Disease and patient characteristics in NP-C patients: findings from an international disease registry
por: Patterson, Marc C, et al.
Publicado: (2013)

Stable or improved neurological manifestations during miglustat therapy in patients from the international disease registry for Niemann-Pick disease type C: an observational cohort study
por: Patterson, Marc C, et al.
Publicado: (2015)

Treatment outcomes following continuous miglustat therapy in patients with Niemann-Pick disease Type C: a final report of the NPC Registry
por: Patterson, Marc C., et al.
Publicado: (2020)

Clinical disease characteristics of patients with Niemann-Pick Disease Type C: findings from the International Niemann-Pick Disease Registry (INPDR)
por: Bolton, Shaun C., et al.
Publicado: (2022)

A Suspicion Index to aid screening of early-onset Niemann-Pick disease Type C (NP-C)
por: Pineda, Mercedes, et al.
Publicado: (2016)

Diagnosis and treatment trends in mucopolysaccharidosis I: findings from the MPS I Registry
por: D’Aco, Kristin, et al.
Publicado: (2012)

Long‐term survival outcomes of patients with Niemann‐Pick disease type C receiving miglustat treatment: A large retrospective observational study
por: Patterson, Marc C., et al.
Publicado: (2020)

Miglustat in Niemann-Pick disease type C patients: a review
por: Pineda, Mercè, et al.
Publicado: (2018)

Oculomotor and Vestibular Findings in Gaucher Disease Type 3 and Their Correlation with Neurological Findings
por: Bremova-Ertl, Tatiana, et al.
Publicado: (2018)

Clinical patient registry recruitment and retention: a survey of patients in two chronic disease registries
por: Solomon, Daniel H., et al.
Publicado: (2017)

Demographic, clinical and antibody characteristics of patients with digital ulcers in systemic sclerosis: data from the DUO Registry
por: Denton, Christopher P, et al.
Publicado: (2012)

Genotype‐phenotype relationships in mucopolysaccharidosis type I (MPS I): Insights from the International MPS I Registry
por: Clarke, Lorne A., et al.
Publicado: (2019)

The disease course of Castleman disease patients with fatal outcomes in the ACCELERATE registry
por: Fajgenbaum, David C., et al.
Publicado: (2022)

Clinical characteristics and predictors of gangrene in patients with systemic sclerosis and digital ulcers in the Digital Ulcer Outcome Registry: a prospective, observational cohort
por: Allanore, Yannick, et al.
Publicado: (2016)

Genetic screening for Niemann–Pick disease type C in adults with neurological and psychiatric symptoms: findings from the ZOOM study
por: Bauer, Peter, et al.
Publicado: (2013)

Development and Implementation of the AIDA International Registry for Patients With Still's Disease
por: Vitale, Antonio, et al.
Publicado: (2022)

Development and implementation of the AIDA International Registry for patients with Behçet’s disease
por: Vitale, Antonio, et al.
Publicado: (2022)

The patient journey of patients with Fabry disease, Gaucher disease and Mucopolysaccharidosis type II: A German-wide telephone survey
por: Mengel, Eugen, et al.
Publicado: (2020)

Prevalence of symptoms in female Fabry disease patients: a case-control survey
por: Bouwman, Machtelt G., et al.
Publicado: (2012)

Learning from disease registries during a pandemic: Moving toward an international federation of patient registries
por: Wall, Dmitri, et al.
Publicado: (2021)

Normalisation of brain spectroscopy findings in Niemann–Pick disease type C patients treated with miglustat
por: Sedel, Frédéric, et al.
Publicado: (2016)

NP-59 Scintigraphy for Primary Aldosteronism Lateralization in a Patient With Polycystic Kidney Disease
por: Fischer, Matan, et al.
Publicado: (2023)

Elucidating the burden of recurrent and chronic digital ulcers in systemic sclerosis: long-term results from the DUO Registry
por: Matucci-Cerinic, Marco, et al.
Publicado: (2016)

Consensus clinical management guidelines for Niemann-Pick disease type C
por: Geberhiwot, Tarekegn, et al.
Publicado: (2018)

Light NP
por: Bishara, Fady
Publicado: (2017)

ProtoDUNE Final Structure for NP02 and NP04
por: Ordan, Julien Marius
Publicado: (2018)

The French Gaucher’s disease registry: clinical characteristics, complications and treatment of 562 patients
por: Stirnemann, Jérôme, et al.
Publicado: (2012)

Reducing posttraumatic stress in parents of patients with a rare inherited metabolic disorder using eye movement desensitization and reprocessing therapy: a case study
por: Conijn, Thirsa, et al.
Publicado: (2021)

Kawasaki Disease in the Time of COVID-19 and MIS-C – The International Kawasaki Disease Registry
por: Harahsheh, Ashraf S., et al.
Publicado: (2023)

Failure to shorten the diagnostic delay in two ultra-orphan diseases (mucopolysaccharidosis types I and III): potential causes and implications
por: Kuiper, Gé-Ann, et al.
Publicado: (2018)

Cognitive development in patients with Mucopolysaccharidosis type III (Sanfilippo syndrome)
por: Valstar, Marlies J, et al.
Publicado: (2011)

Are objective ‘findings’ the same as subjective ‘severity’? A study of the relationship between computed tomography findings and subjective severity in preoperative CRSwNP patients
por: Lu, Hanyu, et al.
Publicado: (2020)

Comparing Natural Product (NP) and non-NP datasets at an atomic scale
por: Heintz, Tobias, et al.
Publicado: (2008)

Development and Implementation of the AIDA International Registry for Patients With Undifferentiated Systemic AutoInflammatory Diseases
por: Della Casa, Francesca, et al.
Publicado: (2022)

Autonomic neuropathy in Fabry disease: a prospective study using the Autonomic Symptom Profile and cardiovascular autonomic function tests
por: Biegstraaten, Marieke, et al.
Publicado: (2010)

Therapy of autoinflammatory diseases: results from an international registry
por: ter Haar, NM, et al.
Publicado: (2011)

Phenotypic diversity in an international Cure VCP Disease registry
por: Ikenaga, Chiseko, et al.
Publicado: (2020)

A potential role for muscle in glucose homeostasis: in vivo kinetic studies in glycogen storage disease type 1a and fructose-1,6-bisphosphatase deficiency
por: Huidekoper, Hidde H., et al.
Publicado: (2010)

The NP Electronics Group
Publicado: (1963)

Physique Nucléaire (NP)
Publicado: (1964)

Cannot write session to /tmp/vufind_sessions/sess_80rp1ve8aak6g6831cjs82tui5