Kristin Ørstavik
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Author network for Kristin Ørstavik by COREMINE medical


Publications 2016

Arntzen KA, Lund I, Rasmussen M, Rønningen KE, Torp TI, Ørstavik K (2016)
[Together for patients with hereditary neuromuscular conditions]
Tidsskr Nor Laegeforen, 136 (14-15), 1198-9
PubMed 27554555

Kist AM, Sagafos D, Rush AM, Neacsu C, Eberhardt E, Schmidt R, Lunden LK, Ørstavik K, Kaluza L, Meents J, Zhang Z, Carr TH, Salter H, Malinowsky D, Wollberg P, Krupp J, Kleggetveit IP, Schmelz M, Jørum E, Lampert A, Namer B (2016)
SCN10A Mutation in a Patient with Erythromelalgia Enhances C-Fiber Activity Dependent Slowing
PLoS One, 11 (9), e0161789
PubMed 27598514

Pedurupillay CR, Amundsen SS, Barøy T, Rasmussen M, Blomhoff A, Stadheim BF, Ørstavik K, Holmgren A, Iqbal T, Frengen E, Misceo D, Strømme P (2016)
Clinical and molecular characteristics in three families with biallelic mutations in IGHMBP2
Neuromuscul Disord, 26 (9), 570-5
PubMed 27450922

Solbakken G, Ørstavik K, Hagen T, Dietrichs E, Naerland T (2016)
Major involvement of trunk muscles in myotonic dystrophy type 1
Acta Neurol Scand, 134 (6), 467-473
PubMed 26984572

Solbakken G, Ørstavik K, Hagen T, Dietrichs E, Nærland T (2016)
Major involvement of trunk muscles in myotonic dystrophy type 1
Acta Neurologica Scandinavica, 1, 1-7
PublikaID 229

Publications 2015

Halvorsen JA, Ørstavik K (2015)
[J.A. Halvorsen & K. Ørstavik reply]
Tidsskr Nor Laegeforen, 135 (20), 1816
PubMed 26534802

Halvorsen JA, Ørstavik K (2015)
[A woman in her 60s with itching arms]
Tidsskr Nor Laegeforen, 135 (16), 1459-61
PubMed 26356457

Namer B, Ørstavik K, Schmidt R, Kleggetveit IP, Weidner C, Mørk C, Kvernebo MS, Kvernebo K, Salter H, Carr TH, Segerdahl M, Quiding H, Waxman SG, Handwerker HO, Torebjörk HE, Jørum E, Schmelz M (2015)
Specific changes in conduction velocity recovery cycles of single nociceptors in a patient with erythromelalgia with the I848T gain-of-function mutation of Nav1.7
Pain, 156 (9), 1637-46
PubMed 25993546

Ørstavik K, Wallace SC, Torbergsen T, Abicht A, Erik Tangsrud S, Kerty E, Rasmussen M (2015)
A de novo Mutation in the SCN4A Gene Causing Sodium Channel Myotonia
J Neuromuscul Dis, 2 (2), 181-184
PubMed 27858731

Publications 2014

Namer B, Schick M, Kleggetveit IP, Ørstavik K, Schmidt R, Jorum E, Torebjörk E, Handwerker H, Schmelz M (2014)
Differential sensitization of silent nociceptors to low pH stimulation by prostaglandin E2 in human volunteers
Eur J Pain, 19 (2), 159-66
PubMed 24890616

Publications 2013

Jørum E, Warncke T, Ørstavik K (2013)
[Small-fibre neuropathy]
Tidsskr Nor Laegeforen, 133 (2), 179-83
PubMed 23344604

Ørstavik K, Kleggetveit IP, Jørum E (2013)
[Microneurography and research on peripheral neuropathic pain]
Tidsskr Nor Laegeforen, 133 (3), 302-5
PubMed 23381167

Publications 2012

Kleggetveit IP, Namer B, Schmidt R, Helås T, Rückel M, Ørstavik K, Schmelz M, Jørum E (2012)
High spontaneous activity of C-nociceptors in painful polyneuropathy
Pain, 153 (10), 2040-7
PubMed 22986070

Ørstavik K, Svalheim S, Gunnarsson R, Gilboe IM, Torbergsen T (2012)
[A seriously ill patient who does not wake up after mechanical ventilation]
Tidsskr Nor Laegeforen, 132 (7), 822-5
PubMed 22511094

Østern R, Fagerheim T, Ørstavik K, Holmøy T, Heiberg A, Lund-Petersen I, Strom TM, Nilssen Ø, Dahl A (2012)
Hereditary motor neuron disease in a large Norwegian family with a "H46R" substitution in the superoxide dismutase 1 gene
Neuromuscul Disord, 22 (6), 511-21
PubMed 22475618

Publications 2009

Orstavik K, Jørum E (2009)
Microneurographic findings of relevance to pain in patients with erythromelalgia and patients with diabetic neuropathy
Neurosci Lett, 470 (3), 180-4
PubMed 19481586

Publications 2008

Namer B, Barta B, Ørstavik K, Schmidt R, Carr R, Schmelz M, Handwerker HO (2008)
Microneurographic assessment of C-fibre function in aged healthy subjects
J Physiol, 587 (2), 419-28
PubMed 19064617

Publications 2007

Namer B, Hilliges M, Orstavik K, Schmidt R, Weidner C, Torebjörk E, Handwerker H, Schmelz M (2007)
Endothelin 1 activates and sensitizes human C-nociceptors
Pain, 137 (1), 41-9
PubMed 17884295

Publications 2006

Jørum E, Ørstavik K, Schmidt R, Namer B, Carr RW, Kvarstein G, Hilliges M, Handwerker H, Torebjörk E, Schmelz M (2006)
Catecholamine-induced excitation of nociceptors in sympathetically maintained pain
Pain, 127 (3), 296-301
PubMed 16997471

Ørstavik K, Namer B, Schmidt R, Schmelz M, Hilliges M, Weidner C, Carr RW, Handwerker H, Jørum E, Torebjörk HE (2006)
Abnormal function of C-fibers in patients with diabetic neuropathy
J Neurosci, 26 (44), 11287-94
PubMed 17079656

Ørstavik K, Norheim I, Jørum E (2006)
Pain and small-fiber neuropathy in patients with hypothyroidism
Neurology, 67 (5), 786-91
PubMed 16966538

Publications 2004

Orstavik K, Mørk C, Kvernebo K, Jørum E (2004)
Pain in primary erythromelalgia--a neuropathic component?
Pain, 110 (3), 531-8
PubMed 15288393

Publications 2003

Schmelz M, Hilliges M, Schmidt R, Ørstavik K, Vahlquist C, Weidner C, Handwerker HO, Torebjörk HE (2003)
Active "itch fibers" in chronic pruritus
Neurology, 61 (4), 564-6
PubMed 12939442

Ørstavik K, Weidner C, Schmidt R, Schmelz M, Hilliges M, Jørum E, Handwerker H, Torebjörk E (2003)
Pathological C-fibres in patients with a chronic painful condition
Brain, 126 (Pt 3), 567-78
PubMed 12566278

Publications 2002

Hilliges M, Weidner C, Schmelz M, Schmidt R, Orstavik K, Torebjork E, Handwerker H (2002)
ATP responses in human C nociceptors
Pain, 98 (1-2), PII S0304-3959(01)00469-9-68

Hilliges M, Weidner C, Schmelz M, Schmidt R, Ørstavik K, Torebjörk E, Handwerker H (2002)
ATP responses in human C nociceptors
Pain, 98 (1-2), 59-68
PubMed 12098617

Weidner C, Schmelz M, Schmidt R, Hammarberg B, Orstavik K, Hilliges M, Torebjörk HE, Handwerker HO (2002)
Neural signal processing: the underestimated contribution of peripheral human C-fibers
J Neurosci, 22 (15), 6704-12
PubMed 12151549

Publications 2001

Ørstavik K, Skard Heier M, Young P, Stögbauer F (2001)
Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsies
Muscle Nerve, 24 (8), 1093-6
PubMed 11439387

Publications 1997

Orstavik K, Ro H, Orstavik KH (1997)
Recurrent brachial plexus neuropathy in a family with subtle dysmorphic features -- a case of hereditary neuralgic amyotrophy
Clin Genet, 51 (6), 421-5
PubMed 9237508

Publications 1975

Orstavik K, Osterud B (1975)
Proceedings: Electroimmunoassay of human coagulation factor IX in the detection of variants of haemophilia B
Thromb Diath Haemorrh, 34 (1), 322-3
PubMed 1188733