SCI Abstract

search
+
Patient and caregiver experiences with a patient-support program for setmelanotide treatment of patients with Bardet–Biedl syndrome
Patient and caregiver experiences with a patient-support program for setmelanotide treatment of patients with Bardet–Biedl syndrome
Bardet–Biedl syndrome (BBS) is a rare genetic disease caused by impaired cilium function and characterized by a plet...
Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosis
Comparison of two genetic strategies for diagnostic work-up of hypertrophic cardiomyopathy: impact on the diagnosis of Fabry disease or transthyretin amyloidosis
Diagnostic work-up of patients with hypertrophic cardiomyopathy is crucial for appropriate management. However, the optima...
Liver transplantation in Wilson disease: a single-center experience
Liver transplantation in Wilson disease: a single-center experience
Wilson disease is a complex genetic disorder due to copper accumulation, mainly in the liver and brain. It is associated w...
Hyperthermic intraperitoneal chemotherapy in patients with incomplete cytoreduction for appendiceal pseudomyxoma peritonei: a 10-year treatment experience in China
Hyperthermic intraperitoneal chemotherapy in patients with incomplete cytoreduction for appendiceal pseudomyxoma peritonei: a 10-year treatment experience in China
To explore the application value of hyperthermic intraperitoneal chemotherapy (HIPEC) in patients with incomplete cytoredu...
Design of mobile and website health application devices for drug tolerability in hereditary fructose intolerance
Design of mobile and website health application devices for drug tolerability in hereditary fructose intolerance
Hereditary fructose intolerance (HFI) is a rare metabolic disease caused by aldolase B deficiency. The aim of our study wa...
Impact of lipodystrophy on health-related quality of life: the QuaLip study
Impact of lipodystrophy on health-related quality of life: the QuaLip study
Lipodystrophy is a rare disease characterized by loss of adipose tissue. Natural history studies have demonstrated signifi...
Development and evaluation of a patient-reported outcome measure specific for Gaucher disease with or without neurological symptoms in Japan
Development and evaluation of a patient-reported outcome measure specific for Gaucher disease with or without neurological symptoms in Japan
Patients with Gaucher disease (GD), a rare lysosomal storage disorder, have reduced health-related quality of life (HRQOL)...
Dysregulation of extracellular matrix and Lysyl Oxidase in Ehlers-Danlos syndrome type IV skin fibroblasts
Dysregulation of extracellular matrix and Lysyl Oxidase in Ehlers-Danlos syndrome type IV skin fibroblasts
Ehlers-Danlos syndrome Type IV (aka Vascular Ehlers Danlos, or vEDS) is a dominantly inherited mutation in the Collagen 3A...
∆4-3-oxo-5β-reductase deficiency: favorable outcome in 16 patients treated with cholic acid
∆4-3-oxo-5β-reductase deficiency: favorable outcome in 16 patients treated with cholic acid
Oral cholic acid therapy is an effective therapy in children with primary bile acid synthesis deficiencies. Most reported ...
Impact of specialist ataxia centres on health service resource utilisation and costs across Europe: cross-sectional survey
Impact of specialist ataxia centres on health service resource utilisation and costs across Europe: cross-sectional survey
Little is known about the costs of treating ataxia and whether treatment at a specialist ataxia centre affects the cost of...
Association of preoperative retinal microcirculation and perioperative outcomes in patients undergoing congenital cardiac surgery
Association of preoperative retinal microcirculation and perioperative outcomes in patients undergoing congenital cardiac surgery
Microcirculatory dysfunction is associated with increased morbidity and mortality in cardiac surgery patients. This study ...
Clinical features of acute attacks, chronic symptoms, and long-term complications among patients with acute hepatic porphyria in Japan: a real-world claims database study
Clinical features of acute attacks, chronic symptoms, and long-term complications among patients with acute hepatic porphyria in Japan: a real-world claims database study
Acute hepatic porphyria (AHP) is a family of rare genetic diseases, including acute intermittent porphyria, variegate porp...
Higher dose alglucosidase alfa is associated with improved overall survival in infantile-onset Pompe disease (IOPD): data from the Pompe Registry
Higher dose alglucosidase alfa is associated with improved overall survival in infantile-onset Pompe disease (IOPD): data from the Pompe Registry
Studies indicate that doses of alglucosidase alfa (ALGLU) higher than label dose (20 mg/kg every other week) impr...
Continued improvement in disease manifestations of acid sphingomyelinase deficiency for adults with up to 2 years of olipudase alfa treatment: open-label extension of the ASCEND trial
Continued improvement in disease manifestations of acid sphingomyelinase deficiency for adults with up to 2 years of olipudase alfa treatment: open-label extension of the ASCEND trial
Olipudase alfa is a recombinant human acid sphingomyelinase enzyme replacement therapy for non-central-nervous-system mani...
Effectiveness and safety of everolimus treatment in patients with tuberous sclerosis complex in real-world clinical practice
Effectiveness and safety of everolimus treatment in patients with tuberous sclerosis complex in real-world clinical practice
The randomised double-blinded placebo-controlled EXIST-1–3 studies have showed everolimus effective with adverse eff...
Parental experiences and needs of caring for a child with 22q11.2 deletion syndrome
Parental experiences and needs of caring for a child with 22q11.2 deletion syndrome
For a variety of reasons, raising a child with 22q11.2DS has significant psychosocial and financial repercussions for the ...
Clinical and genetic profiles of chinese pediatric patients with catecholaminergic polymorphic ventricular tachycardia
Clinical and genetic profiles of chinese pediatric patients with catecholaminergic polymorphic ventricular tachycardia
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a rare but lethal cardiac ion channelopathy. Delayed diagn...
Using theory of change to co-create a programme theory for a telerehabilitation intervention for pain management in people with haemophilia
Using theory of change to co-create a programme theory for a telerehabilitation intervention for pain management in people with haemophilia
Improved approaches for chronic pain management are a clinical and research priority for people with haemophilia (PWH). In...
The improvement of motor symptoms in Huntington’s disease during cariprazine treatment
The improvement of motor symptoms in Huntington’s disease during cariprazine treatment
Huntington’s disease (HD) is a progressive neurodegenerative disease, characterised by motor disturbances and non-mo...
Self-reported functioning among patients with ultra-rare nemaline myopathy or a related disorder in Finland: a pilot study
Self-reported functioning among patients with ultra-rare nemaline myopathy or a related disorder in Finland: a pilot study
Nemaline myopathy (NM) and related disorders (NMr) form a heterogenous group of ultra-rare (1:50,000 live births or less) ...
Clinical features, genomic profiling, and outcomes of adult patients with unifocal Langerhans cell histiocytosis
Clinical features, genomic profiling, and outcomes of adult patients with unifocal Langerhans cell histiocytosis
Langerhans cell histiocytosis (LCH) is a rare highly heterogeneous histiocytosis, which can be divided into single system ...
Qualified placebo for trials of herbal medicine treatment in rare diseases? A cross-sectional analysis
Qualified placebo for trials of herbal medicine treatment in rare diseases? A cross-sectional analysis
While substantial placebos have been used in herbal medicine (HM) clinical trials for rare diseases, the use and quality o...
Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine
Identification of novel homozygous nonsense SLC10A7 variant causing short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis and surgical management of spine
Short stature, amelogenesis imperfecta, and skeletal dysplasia with scoliosis is a rare, autosomal recessive, skeletal dis...
Correction: Meeting abstracts from the 11th edition of the European conference on Rare Diseases & Orphan Products (ECRD) 2022
Correction: Meeting abstracts from the 11th edition of the European conference on Rare Diseases & Orphan Products (ECRD) 2022
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, whi...
Efficacy and safety of compassionate use for rare diseases: a scoping review from 1991 to 2022
Efficacy and safety of compassionate use for rare diseases: a scoping review from 1991 to 2022
Compassionate use is a system that provides patients with expedited access to drugs which has not yet been approved, but c...
Explorative research on glucolipid metabolism and levels of adipokines in pseudohypoparathyroidism type 1 patients
Explorative research on glucolipid metabolism and levels of adipokines in pseudohypoparathyroidism type 1 patients
Pseudohypoparathyroidism type 1 (PHP1) is a rare disease featuring hypocalcemia and elevated PTH level. Though disturbed c...
Correction: Expert Group Consensus on early diagnosis and management of infantile-onset pompe disease in the Gulf Region
Correction: Expert Group Consensus on early diagnosis and management of infantile-onset pompe disease in the Gulf Region
Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, whi...
Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals
Experiences of coordinated care for people in the UK affected by rare diseases: cross-sectional survey of patients, carers, and healthcare professionals
Poorly coordinated care can have major impacts on patients and families affected by rare conditions, with negative physica...
Prioritization of research engaged with rare disease stakeholders: a systematic review and thematic analysis
Prioritization of research engaged with rare disease stakeholders: a systematic review and thematic analysis
Although rare diseases (RD) are increasingly becoming a priority for healthcare activities and services around the world, ...
Educational needs of patients, families, and healthcare professionals to support the patient journey in haemophilia gene therapy in the UK
Educational needs of patients, families, and healthcare professionals to support the patient journey in haemophilia gene therapy in the UK
With the first gene therapies for haemophilia approved by the European Commission, the US Food and Drug Administration, an...
Load More
format_indent_increase