Pages that link to "Q37957492"
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The following pages link to Familial amyloid polyneuropathy (Q37957492):
Displaying 50 items.
- Mechanism of Action and Clinical Application of Tafamidis in Hereditary Transthyretin Amyloidosis (Q26764754) (← links)
- The clinical approach to small fibre neuropathy and painful channelopathy (Q26863734) (← links)
- The role of tau in neurodegenerative diseases and its potential as a therapeutic target (Q27005032) (← links)
- Recommendations for presymptomatic genetic testing and management of individuals at risk for hereditary transthyretin amyloidosis (Q28076550) (← links)
- Sixty years of transthyretin familial amyloid polyneuropathy (TTR-FAP) in Europe: where are we now? A European network approach to defining the epidemiology and management patterns for TTR-FAP (Q28078350) (← links)
- Evolving landscape in the management of transthyretin amyloidosis (Q28086773) (← links)
- The Reg3α (HIP/PAP) Lectin Suppresses Extracellular Oxidative Stress in a Murine Model of Acute Liver Failure (Q28546990) (← links)
- Transthyretin-Related Familial Amyloid Polyneuropathy (TTR-FAP): A Single-Center Experience in Sicily, an Italian Endemic Area (Q29248271) (← links)
- Hereditary Transthyretin Amyloidosis in Eight Chinese Families. (Q30386725) (← links)
- Transthyretin variants with improved inhibition of β-amyloid aggregation (Q30757280) (← links)
- Safety and efficacy of long-term diflunisal administration in hereditary transthyretin (ATTR) amyloidosis (Q33423160) (← links)
- Gene expression profile in hereditary transthyretin amyloidosis: differences in targeted and source organs (Q33716349) (← links)
- Corino de Andrade disease: mechanisms and impact on reproduction (Q33807480) (← links)
- Abnormal expression of homeobox genes and transthyretin in C9ORF72 expansion carriers (Q33821516) (← links)
- Small-fibre neuropathies--advances in diagnosis, pathophysiology and management (Q34277762) (← links)
- Update in the diagnosis and management of transthyretin familial amyloid polyneuropathy (Q34422510) (← links)
- An overview of drugs currently under investigation for the treatment of transthyretin-related hereditary amyloidosis (Q34428314) (← links)
- Curcumin could reduce the monomer of TTR with Tyr114Cys mutation via autophagy in cell model of familial amyloid polyneuropathy (Q34464337) (← links)
- Binding site asymmetry in human transthyretin: insights from a joint neutron and X-ray crystallographic analysis using perdeuterated protein (Q34473216) (← links)
- Allele specific expression of the transthyretin gene in swedish patients with hereditary transthyretin amyloidosis (ATTR V30M) is similar between the two alleles (Q34490823) (← links)
- Neurophysiological markers of small fibre neuropathy in TTR-FAP mutation carriers (Q34544072) (← links)
- Recent advances in transthyretin amyloidosis therapy (Q34664696) (← links)
- ANO5-muscular dystrophy: clinical, pathological and molecular findings (Q34714751) (← links)
- Neurophysiological techniques to detect early small-fiber dysfunction in transthyretin amyloid polyneuropathy. (Q34726962) (← links)
- A woman with a rare p.Glu74Gly transthyretin mutation presenting exclusively with a rapidly progressive neuropathy: a case report (Q34894825) (← links)
- Oculoleptomeningeal Amyloidosis associated with transthyretin Leu12Pro in an African patient (Q34907093) (← links)
- Structure-based analysis of A19D, a variant of transthyretin involved in familial amyloid cardiomyopathy (Q35072784) (← links)
- In vivo detection of nerve injury in familial amyloid polyneuropathy by magnetic resonance neurography (Q35119383) (← links)
- Cardiac findings and events observed in an open-label clinical trial of tafamidis in patients with non-Val30Met and non-Val122Ile hereditary transthyretin amyloidosis (Q35244195) (← links)
- Post hoc analysis of nutritional status in patients with transthyretin familial amyloid polyneuropathy: impact of tafamidis. (Q35280661) (← links)
- Macular and optic disc edema and retinal vascular leakage in familial amyloid polyneuropathy with a transthyretin Val30Met mutation: a case report (Q35302228) (← links)
- Computational re-engineering of Amylin sequence with reduced amyloidogenic potential (Q35612061) (← links)
- Systemic organ wasting induced by localized expression of the secreted insulin/IGF antagonist ImpL2. (Q35623178) (← links)
- IgG Conformer's Binding to Amyloidogenic Aggregates (Q35772596) (← links)
- The Temporal Profiles of Changes in Nerve Excitability Indices in Familial Amyloid Polyneuropathy (Q35830457) (← links)
- Neuropathologic analysis of Tyr69His TTR variant meningovascular amyloidosis with dementia (Q35834448) (← links)
- Intermediate Charcot-Marie-Tooth disease due to a novel Trp101Stop myelin protein zero mutation associated with debilitating neuropathic pain. (Q36103150) (← links)
- A New Folding Kinetic Mechanism for Human Transthyretin and the Influence of the Amyloidogenic V30M Mutation. (Q36121846) (← links)
- Population diversity of the genetically determined TTR expression in human tissues and its implications in TTR amyloidosis (Q36320893) (← links)
- Transthyretin (TTR) cardiac amyloidosis (Q36408438) (← links)
- Amyloid neuropathies (Q36493200) (← links)
- Clinical, ECG and echocardiographic clues to the diagnosis of TTR-related cardiomyopathy (Q36559736) (← links)
- Endoscopic Findings of Small-Bowel Lesions in Familial Amyloid Polyneuropathy: A Case Report. (Q36822622) (← links)
- Exome Sequencing and Gene Prioritization Correct Misdiagnosis in a Chinese Kindred with Familial Amyloid Polyneuropathy (Q36925525) (← links)
- Sudomotor innervation in transthyretin amyloid neuropathy: Pathology and functional correlates. (Q37279325) (← links)
- Effects of tafamidis on transthyretin stabilization and clinical outcomes in patients with non-Val30Met transthyretin amyloidosis (Q37337552) (← links)
- Induced pluripotent stem cell modeling of multisystemic, hereditary transthyretin amyloidosis. (Q37344629) (← links)
- A novel prion disease associated with diarrhea and autonomic neuropathy (Q37393739) (← links)
- Ophthalmic manifestations in a Chinese family with familial amyloid polyneuropathy due to a TTR Gly83Arg mutation (Q37474592) (← links)
- Epidemiology of transthyretin-associated familial amyloid polyneuropathy in the Majorcan area: Son Llàtzer Hospital descriptive study (Q37615767) (← links)