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Umeå universitet
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Intissar Anan

Kontakt

E-post
intissar.anan@umu.se

Verksam vid

Anknytning
Anknuten som övrig/annan befattning till Wallenberg centrum för molekylär medicin vid Umeå universitet (WCMM)
Plats
Umeå universitet, 901 87 Umeå
Anknytning
Anknuten som läkare till Institutionen för folkhälsa och klinisk medicin Enhet: Avdelningen för medicin
Plats
1A, målpunkt B41, plan 4, Norrlands universitetssjukhus Norrlands universitetssjukhus, 90185 Umeå
2019
A case report of osteoarthritis associated with hereditary transthyretin amyloidosis ATTRV30M
Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2019, Vol. 26 : 29-30
Anan, Intissar; Bång, Joakim; Lundgren, Hans-Erik; et al.
2019
Transthyretin Glu54Leu - an unknown mutation within the Swedish population associated with amyloid cardiomyopathy and a unique fibril type
Scandinavian Journal of Clinical and Laboratory Investigation, Taylor & Francis 2019, Vol. 79, (6) : 372-376
Hellman, Urban; Lång, Kenneth; Ihse, Elisabet; et al.
2019
Prevalence of transthyretin cardiac amyloidosis in a community-based heart failure population
European Heart Journal, Oxford University Press 2019, Vol. 40 : 132-132
Lindmark, Krister; Pilebro, Björn; Solekrans, L.; et al.
2019
Self-reported gastrointestinal symptoms are more common in liver transplanted transthyretin amyloidosis patients than in healthy controls and in patients transplanted for end-stage liver disease
Amyloid: Journal of Protein Folding Disorders, Taylor & Francis 2019, Vol. 26 : 47-48
Marberg, Therese; Karling, Pontus; Söderberg, Karin; et al.
2019
Amyloid fibril composition within hereditary Val30Met (p. Val50Met) transthyretin amyloidosis families
PLoS ONE, Public Library Science 2019, Vol. 14, (2)
Suhr, Ole Bernt; Wixner, Jonas; Anan, Intissar; et al.
2019
Visualisation of amyloid deposition within the brain of long-term hereditary transthyretin amyloidosis survivors by 18F-flutemetamol positron emission tomography
European Journal of Neurology, John Wiley & Sons 2019, Vol. 26, (S1) : 287-287
Unéus, Erica; Wilhelmsson, Christer; Suhr, Ole; et al.
2019
The Swedish open-label diflunisal trial (DFNS01) on hereditary transthyretin amyloidosis and the impact of amyloid fibril composition
Amyloid: Journal of Protein Folding Disorders, Taylor & Francis Group 2019, Vol. 26 : 39-40
Wixner, Jonas; Westermark, Per; Ihse, Elisabet; et al.
2018
Atrial Fibrillation and Central Nervous Complications in Liver Transplanted Hereditary Transthyretin Amyloidosis Patients
Transplantation, LIPPINCOTT WILLIAMS & WILKINS 2018, Vol. 102, (2) : e59-e66
Wange, Niklas; Anan, Intissar; Ericzon, Bo-Göran; et al.
2018
Management of gastrointestinal complications in hereditary transthyretin amyloidosis: a single-center experience over 40 years
Expert Review of Gastroenterology & Hepatology, Taylor & Francis 2018, Vol. 12, (1) : 73-81
Wixner, Jonas; Suhr, Ole B.; Anan, Intissar
2018
Abnormal small bowel motility in patients with hereditary transthyretin amyloidosis
Neurogastroenterology and Motility, Wiley-Blackwell 2018, Vol. 30, (9)
Wixner, Jonas; Törnblom, H.; Karling, Pontus; et al.
2017
The Swedish landscape of hereditary ATTR amyloidosis
Amyloid: Journal of Protein Folding Disorders, Vol. 24, (1) : 93-94
Suhr, Ole B; Wixner, Jonas; Pilebro, Björn; et al.
2017
Effect of doxycycline and ursodeoxycholic acid on transthyretin amyloidosis
Amyloid: Journal of Protein Folding Disorders, Vol. 24, (1) : 78-79
Wixner, Jonas; Pilebro, Bjorn; Lundgren, Hans-Erik; et al.
2015
Enthalpic Forces Correlate with Selectivity of Transthyretin-Stabilizing Ligands in Human Plasma
Journal of Medicinal Chemistry, Vol. 58, (16) : 6507-6515
Iakovleva, Irina; Brännström, Kristoffer; Nilsson, Lina; et al.
2015
Outcome of gastric emptying and gastrointestinal symptoms after liver transplantation for hereditary transthyretin amyloidosis
BMC Gastroenterology, Vol. 15
Wixner, Jonas; Sundström, Torbjorn; Karling, Pontus; et al.
2014
THAOS: Gastrointestinal manifestations of transthyretin amyloidosis - common complications of a rare disease
Orphanet Journal of Rare Diseases, BioMed Central 2014, Vol. 9, (1) : 61-
Wixner, Jonas; Mundayat, Rajiv; Karayal, Onur N; et al.
2013
Impact of antibodies against amyloidogenic transthyretin (ATTR) on phenotypes of patients with familial amyloidotic polyneuropathy (FAP) ATTR Valine30Methionine
Clinica Chimica Acta, Vol. 419C : 127-131
Obayashi, Konen; Tasaki, Masayoshi; Jono, Hirofumi; et al.
2013
Loss of gastric interstitial cells of Cajal in patients with hereditary transthyretin amyloidosis
Amyloid: Journal of Protein Folding Disorders, Informa Healthcare 2013, Vol. 20, (2) : 99-106
Wixner, Jonas; Obayashi, Konen; Ando, Yukio; et al.
2012
Gastric emptying in hereditary transthyretin amyloidosis: the impact of autonomic neuropathy
Neurogastroenterology and Motility, Wiley-Blackwell 2012, Vol. 24, (12) : 1111-e568
Wixner, Jonas; Karling, Pontus; Rydh, Anders; et al.
2010
Serum transthyretin levels in Swedish TTR V30M carriers
Amyloid: Journal of Protein Folding Disorders, Vol. 17, (2) : 83-85
Buxbaum, Joel; Anan, Intissar; Suhr, Ole B
2008
Impact of serotonin transporter and catechol-O-methyl transferase genes polymorphism on gastrointestinal dysfunction in Swedish and Japanese familial amyloidotic polyneuropathy patients.
Clinica Chimica Acta, Vol. 398, (1-2) : 10-4
Obayashi, Konen; Olsson, Malin; Anan, Intissar; et al.
2008
Do troponin and B-natriuretic peptide detect cardiomyopathy in transthyretin amyloidosis?
Journal of Internal Medicine, John Wiley & Sons 2008, Vol. 263, (3) : 294-301
Suhr, Ole B; Anan, Intissar; Backman, Clas; et al.
2005
Cardiomyopathy in Swedish patients with the Gly53Glu and His88Arg transthyretin variants.
Amyloid, Vol. 12, (3) : 184-8
Holmgren, Gösta; Hellman, Urban; Anan, Intissar; et al.
2005
Advanced glycation end product is implicated in amyloid-related kidney complications
Scandinavian Journal of Clinical and Laboratory Investigation, Informa Healthcare 2005, Vol. 65, (4) : 263-272
Matsunaga, N; Anan, Intissar; Rosenberg, P; et al.
2003
Gastric emptying before and after liver transplantation for familial amyloidotic polyneuropathy, Portuguese type (Val30Met).
Amyloid: Journal of Protein Folding Disorders, Vol. 10, (2) : 121-6
Suhr, Ole B; Anan, Intissar; Åhlström Riklund, Katrine; et al.
2002
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-kappaB activation.
Acta Neuropathologica, Vol. 104, (5) : 441-7
Matsunaga, Noriko; Anan, Intissar; Forsgren, Sture; et al.
2002
Reduction of free radical activity in amyloid deposits following liver transplantation for familial amyloidotic polyneuropathy.
Journal of Internal Medicine, Vol. 251, (2) : 136-41
Nyhlin, N; Anan, Intissar; El, Salhy M; et al.
2001
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.
Acta Neuropathologica, Vol. 102, (3) : 227-32
Anan, Intissar; El-salhy, M; Ando, Y; et al.
2001
Scavenger treatment of free radical injury in familial amyloidotic polyneuropathy: a study on Swedish transplanted and non-transplanted patients.
Scandinavian Journal of Clinical and Laboratory Investigation, Vol. 61, (1) : 11-8
Suhr, Ole B; Lång, K; Wikström, L; et al.
2000
Liver transplantation restores endocrine cells in patients with familial amyloidotic polyneuropathy.
Transplantation, Vol. 70, (5) : 794-9
Anan, Intissar; El-Salhy, M; Nyhlin, N; et al.
2000
Heart failure caused by a novel amyloidogenic mutation of the transthyretin gene: ATTR Ala45Ser.
Amyloid: Journal of Protein Folding Disorders, Vol. 7, (2) : 137-40
Janunger, T; Anan, Intissar; Holmgren, G; et al.
2000
Enhancement of AA-amyloid formation in mice by transthyretin amyloid fragments and polyethylene glycol.
Biochimica et Biophysica Acta, Vol. 1474, (3) : 331-6
Mambule, C; Ando, Y; Anan, Intissar; et al.
1999
Colonic enteric nervous system in patients with familial amyloidotic neuropathy.
Acta Neuropathologica, Vol. 98, (1) : 48-54
Anan, Intissar; El-Salhy, M; Ando, Y; et al.
1999
Colonic endocrine cells in patients with familial amyloidotic polyneuropathy.
Journal of Internal Medicine, Vol. 245, (5) : 469-73
Anan, Intissar; El-Salhy, M; Ando, Y; et al.
1999
Endocrine cells in the upper gastrointestinal tract in relation to gastrointestinal dysfunction in patients with familial amyloidotic polyneuropathy.
Amyloid: Journal of Protein Folding Disorders, Vol. 6, (3) : 192-8
Nyhlin, N; Anan, Intissar; el-Salhy, M; et al.
1998
Detection of a variant protein in hair: new diagnostic method in Portuguese type familial amyloid polyneuropathy.
BMJ (Clinical Research Edition), Vol. 316, (7143) : 1500-1
Ando, Y; Anan, Intissar; Suhr, Ole B; et al.
Visa publikationer i DiVA
Publicerad: 07 feb, 2019
Gåtan Skelleftesjukan – på väg att lösas?
Gåtan Skelleftesjukan – på väg att lösas?

Intissar Anan berättar om forskning kring Skelleftesjukan, och om gåtan Skelleftesjukan är på väg att lösas.