Ole Bernt Suhr


Ontology type: schema:Person     


Person Info

NAME

Ole Bernt

SURNAME

Suhr

Publications in SciGraph latest 50 shown

  • 2021-05-25 A human antibody selective for transthyretin amyloid removes cardiac amyloid through phagocytic immune cells in NATURE COMMUNICATIONS
  • 2020-12-26 Cardiac transthyretin amyloidosis 99mTc-DPD SPECT correlates with strain echocardiography and biomarkers in EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
  • 2020-10-08 Abdominal fat pad biopsies exhibit good diagnostic accuracy in patients with suspected transthyretin amyloidosis in ORPHANET JOURNAL OF RARE DISEASES
  • 2020-09-23 Avoiding misdiagnosis: expert consensus recommendations for the suspicion and diagnosis of transthyretin amyloidosis for the general practitioner in BMC PRIMARY CARE
  • 2020-07-08 A phase II, open-label, extension study of long-term patisiran treatment in patients with hereditary transthyretin-mediated (hATTR) amyloidosis in ORPHANET JOURNAL OF RARE DISEASES
  • 2020-01-06 Expert consensus recommendations to improve diagnosis of ATTR amyloidosis with polyneuropathy in JOURNAL OF NEUROLOGY
  • 2019-08-26 Diagnosis and treatment of gastrointestinal dysfunction in hereditary TTR amyloidosis in CLINICAL AUTONOMIC RESEARCH
  • 2017-09-11 Trial design and rationale for APOLLO, a Phase 3, placebo-controlled study of patisiran in patients with hereditary ATTR amyloidosis with polyneuropathy in BMC NEUROLOGY
  • 2016-09-19 Positron emission tomography (PET) utilizing Pittsburgh compound B (PIB) for detection of amyloid heart deposits in hereditary transthyretin amyloidosis (ATTR) in JOURNAL OF NUCLEAR CARDIOLOGY
  • 2015-11-02 Positron Emission Tomography (PET) utilizing Pittsburgh compound B (PIB) detects amyloid heart deposits in hereditary transthyretin amyloidosis (ATTR). in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-11-02 Characterization of conformation-specific, human-derived monoclonal antibodies against TTR aggregates with potential for diagnostic and therapeutic use in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-11-02 Treatment of gastrointestinal complication in transthyretin amyloidosis. A single centre’s experience in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-11-02 Phase 2 open-label extention (OLE) study of patisiran, an investigational siRNA agent for familial amyloidotic polyneuropathy (FAP) in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-11-02 Preliminary assessment of neuropathy progression in patients with hereditary ATTR amyloidosis after orthotopic liver transplantation (OLT) in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-11-02 Delayed small bowel octreotide response in patients with hereditary transthyretin amyloidosis in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-09-04 Efficacy and safety of patisiran for familial amyloidotic polyneuropathy: a phase II multi-dose study in ORPHANET JOURNAL OF RARE DISEASES
  • 2015-04-25 Outcome of gastric emptying and gastrointestinal symptoms after liver transplantation for hereditary transthyretin amyloidosis in BMC GASTROENTEROLOGY
  • 2014-12-11 Post Hoc Analysis of Nutritional Status in Patients with Transthyretin Familial Amyloid Polyneuropathy: Impact of Tafamidis in NEUROLOGY AND THERAPY
  • 2014-04-27 THAOS: Gastrointestinal manifestations of transthyretin amyloidosis - common complications of a rare disease in ORPHANET JOURNAL OF RARE DISEASES
  • 2013-08-22 Long-term effects of tafamidis for the treatment of transthyretin familial amyloid polyneuropathy in JOURNAL OF NEUROLOGY
  • 2010-11-25 Variation in amount of wild-type transthyretin in different fibril and tissue types in ATTR amyloidosis in JOURNAL OF MOLECULAR MEDICINE
  • 2010-10-07 Blood pressure overshoot after tilt reversal in patients with familial amyloidotic polyneuropathy in HYPERTENSION RESEARCH
  • 2010-09-14 A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers in BMC MEDICAL GENOMICS
  • 2010-03-17 TTR familial amyloid polyneuropathy: does a mitochondrial polymorphism entirely explain the parent-of-origin difference in penetrance? in EUROPEAN JOURNAL OF HUMAN GENETICS
  • 2009-07-29 Liver Transplantation for Transthyretin Amyloidosis in RECENT ADVANCES IN TRANSTHYRETIN EVOLUTION, STRUCTURE AND BIOLOGICAL FUNCTIONS
  • 2003-10-08 Sulfite and base for the treatment of familial amyloidotic polyneuropathy: two additive approaches to stabilize the conformation of human amyloidogenic transthyretin in NEUROGENETICS
  • 2002-07-26 Advanced glycation end products (AGE) and the receptor for AGE are present in gastrointestinal tract of familial amyloidotic polyneuropathy patients but do not induce NF-κB activation in ACTA NEUROPATHOLOGICA
  • 2001-09 Comparison of amyloid deposits and infiltration of enteric nervous system in the upper with those in the lower gastrointestinal tract in patients with familial amyloidotic polyneuropathy in ACTA NEUROPATHOLOGICA
  • 1999-06 Colonic enteric nervous system in patients with familial amyloidotic neuropathy in ACTA NEUROPATHOLOGICA
  • 1998-07 Serum amyloid P component scintigraphy in familial amyloid polyneuropathy: regression of visceral amyloid following liver transplantation in EUROPEAN JOURNAL OF NUCLEAR MEDICINE AND MOLECULAR IMAGING
  • 1998-06 Liver transplantation in familial amyloidotic polyneuropathy (FAP). A comparative study of transplanted and non-transplanted patient's survival in TRANSPLANT INTERNATIONAL
  • 1997-02 Evaluation of immunohistochemical staining of human duodenal endocrine cells after microwave antigen retrieval in JOURNAL OF MOLECULAR HISTOLOGY
  • 1996-10 Impact of gastrointestinal dysfunction on survival after liver transplantation for familial amyloidotic polyneuropathy in DIGESTIVE DISEASES AND SCIENCES
  • 1987-01 Nicardipine in the treatment of essential hypertension controlled 6-month-study comparing nicardipine with propranolol at rest and during exercise in EUROPEAN JOURNAL OF CLINICAL PHARMACOLOGY
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