| Year |
Citation |
Score |
| 2019 |
Koskelainen S, Zhao F, Kalimo H, Baumann M, Kiuru-Enari S. Severe elastolysis in hereditary gelsolin (AGel) amyloidosis. Amyloid : the International Journal of Experimental and Clinical Investigation : the Official Journal of the International Society of Amyloidosis. 1-8. PMID 31814469 DOI: 10.1080/13506129.2019.1699785 |
0.314 |
|
| 2019 |
Rajani RM, Ratelade J, Domenga-Denier V, Hase Y, Kalimo H, Kalaria RN, Joutel A. Blood brain barrier leakage is not a consistent feature of white matter lesions in CADASIL. Acta Neuropathologica Communications. 7: 187. PMID 31753008 DOI: 10.1186/S40478-019-0844-X |
0.349 |
|
| 2017 |
Munteanu I, Kalimo H, Saraste A, Nishino I, Minassian BA. Cardiac autophagic vacuolation in severe X-linked myopathy with excessive autophagy. Neuromuscular Disorders. 27: 185-187. PMID 27916343 DOI: 10.1016/J.Nmd.2016.10.007 |
0.347 |
|
| 2016 |
Koskelainen S, Pihlamaa T, Suominen S, Zhao F, Salo T, Risteli J, Baumann M, Kalimo H, Kiuru-Enari S. Gelsolin amyloid angiopathy causes severe disruption of the arterial wall. Apmis : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica. PMID 27198069 DOI: 10.1111/Apm.12554 |
0.35 |
|
| 2015 |
Craggs L, Taylor J, Slade JY, Chen A, Hagel C, Kuhlenbaeumer G, Borjesson-Hanson A, Viitanen M, Kalimo H, Deramecourt V, Oakley AE, Kalaria RN. Clusterin/Apolipoprotein J immunoreactivity is associated with white matter damage in cerebral small vessel diseases. Neuropathology and Applied Neurobiology. PMID 25940137 DOI: 10.1111/Nan.12248 |
0.303 |
|
| 2015 |
Saraste A, Koskenvuo JW, Airaksinen J, Ramachandran N, Munteanu I, Udd B, Huovinen S, Kalimo H, Minassian BA. No cardiomyopathy in X-linked myopathy with excessive autophagy. Neuromuscular Disorders : Nmd. 25: 485-7. PMID 25845477 DOI: 10.1016/J.Nmd.2015.03.003 |
0.322 |
|
| 2015 |
Dowling JJ, Moore SA, Kalimo H, Minassian BA. X-linked myopathy with excessive autophagy: a failure of self-eating. Acta Neuropathologica. 129: 383-90. PMID 25644398 DOI: 10.1007/S00401-015-1393-4 |
0.339 |
|
| 2014 |
Tikka S, Baumann M, Siitonen M, Pasanen P, Pöyhönen M, Myllykangas L, Viitanen M, Fukutake T, Cognat E, Joutel A, Kalimo H. CADASIL and CARASIL. Brain Pathology (Zurich, Switzerland). 24: 525-44. PMID 25323668 DOI: 10.1111/Bpa.12181 |
0.335 |
|
| 2013 |
Järvinen TA, Järvinen M, Kalimo H. Regeneration of injured skeletal muscle after the injury. Muscles, Ligaments and Tendons Journal. 3: 337-45. PMID 24596699 DOI: 10.32098/Mltj.04.2013.16 |
0.305 |
|
| 2013 |
Kalimo H, Lalowski M, Bogdanovic N, Philipson O, Bird TD, Nochlin D, Schellenberg GD, Brundin R, Olofsson T, Soliymani R, Baumann M, Wirths O, Bayer TA, Nilsson LN, Basun H, et al. The Arctic AβPP mutation leads to Alzheimer's disease pathology with highly variable topographic deposition of differentially truncated Aβ. Acta Neuropathologica Communications. 1: 60. PMID 24252272 DOI: 10.1186/2051-5960-1-60 |
0.301 |
|
| 2013 |
Craggs LJ, Hagel C, Kuhlenbaeumer G, Borjesson-Hanson A, Andersen O, Viitanen M, Kalimo H, McLean CA, Slade JY, Hall RA, Oakley AE, Yamamoto Y, Deramecourt V, Kalaria RN. Quantitative vascular pathology and phenotyping familial and sporadic cerebral small vessel diseases. Brain Pathology (Zurich, Switzerland). 23: 547-57. PMID 23387519 DOI: 10.1111/Bpa.12041 |
0.321 |
|
| 2013 |
Ramachandran N, Munteanu I, Wang P, Ruggieri A, Rilstone JJ, Israelian N, Naranian T, Paroutis P, Guo R, Ren ZP, Nishino I, Chabrol B, Pellissier JF, Minetti C, Udd B, ... ... Kalimo H, et al. VMA21 deficiency prevents vacuolar ATPase assembly and causes autophagic vacuolar myopathy. Acta Neuropathologica. 125: 439-57. PMID 23315026 DOI: 10.1007/S00401-012-1073-6 |
0.319 |
|
| 2012 |
Tikka S, Ng YP, Di Maio G, Mykkänen K, Siitonen M, Lepikhova T, Pöyhönen M, Viitanen M, Virtanen I, Kalimo H, Baumann M. CADASIL mutations and shRNA silencing of NOTCH3 affect actin organization in cultured vascular smooth muscle cells. Journal of Cerebral Blood Flow and Metabolism : Official Journal of the International Society of Cerebral Blood Flow and Metabolism. 32: 2171-80. PMID 22948298 DOI: 10.1038/Jcbfm.2012.123 |
0.311 |
|
| 2012 |
Kousi M, Anttila V, Schulz A, Calafato S, Jakkula E, Riesch E, Myllykangas L, Kalimo H, Topçu M, Gökben S, Alehan F, Lemke JR, Alber M, Palotie A, Kopra O, et al. Novel mutations consolidate KCTD7 as a progressive myoclonus epilepsy gene. Journal of Medical Genetics. 49: 391-9. PMID 22693283 DOI: 10.1136/Jmedgenet-2012-100859 |
0.31 |
|
| 2011 |
Arboleda-Velasquez JF, Manent J, Lee JH, Tikka S, Ospina C, Vanderburg CR, Frosch MP, RodrÃguez-Falcón M, Villen J, Gygi S, Lopera F, Kalimo H, Moskowitz MA, Ayata C, Louvi A, et al. Hypomorphic Notch 3 alleles link Notch signaling to ischemic cerebral small-vessel disease. Proceedings of the National Academy of Sciences of the United States of America. 108: E128-35. PMID 21555590 DOI: 10.1073/Pnas.1101964108 |
0.343 |
|
| 2011 |
Hackman P, Sandell S, Sarparanta J, Luque H, Huovinen S, Palmio J, Paetau A, Kalimo H, Mahjneh I, Udd B. Four new Finnish families with LGMD1D; refinement of the clinical phenotype and the linked 7q36 locus. Neuromuscular Disorders : Nmd. 21: 338-44. PMID 21376592 DOI: 10.1016/J.Nmd.2011.02.008 |
0.313 |
|
| 2011 |
Yamamoto Y, Craggs L, Baumann M, Kalimo H, Kalaria RN. Review: molecular genetics and pathology of hereditary small vessel diseases of the brain. Neuropathology and Applied Neurobiology. 37: 94-113. PMID 21062344 DOI: 10.1111/J.1365-2990.2010.01147.X |
0.335 |
|
| 2010 |
Sundblom J, Stålberg E, Osterdahl M, Rücker F, Montelius M, Kalimo H, Nennesmo I, Islander G, Smits A, Dahl N, Melberg A. Bedside diagnosis of rippling muscle disease in CAV3 p.A46T mutation carriers. Muscle & Nerve. 41: 751-7. PMID 20229577 DOI: 10.1002/Mus.21589 |
0.342 |
|
| 2010 |
Melberg A, Kretz C, Kalimo H, Wallgren-Pettersson C, Toussaint A, Böhm J, Stålberg E, Laporte J. Adult course in dynamin 2 dominant centronuclear myopathy with neonatal onset. Neuromuscular Disorders : Nmd. 20: 53-6. PMID 19932619 DOI: 10.1016/J.Nmd.2009.10.006 |
0.34 |
|
| 2009 |
Ramachandran N, Munteanu I, Wang P, Aubourg P, Rilstone JJ, Israelian N, Naranian T, Paroutis P, Guo R, Ren ZP, Nishino I, Chabrol B, Pellissier JF, Minetti C, Udd B, ... ... Kalimo H, et al. VMA21 deficiency causes an autophagic myopathy by compromising V-ATPase activity and lysosomal acidification. Cell. 137: 235-46. PMID 19379691 DOI: 10.1016/J.Cell.2009.01.054 |
0.318 |
|
| 2009 |
Paljärvi L, Karjalainen K, Kalimo H. Lectin Histochemistry Of Normal And Diseased Human Muscle Acta Neurologica Scandinavica. 65: 248-249. DOI: 10.1111/J.1600-0404.1982.Tb03474.X |
0.309 |
|
| 2008 |
Eeg-Olofsson O, Kalimo H, Eeg-Olofsson KE, Jagell S, Marklund L, Simonsson L, Dahl N. Duchenne muscular dystrophy and idiopathic hyperCKemia in the same family. European Journal of Paediatric Neurology : Ejpn : Official Journal of the European Paediatric Neurology Society. 12: 404-7. PMID 18833644 DOI: 10.1016/J.Ejpn.2007.10.014 |
0.305 |
|
| 2008 |
Kalimo H, Miao Q, Tikka S, Mykkänen K, Junna M, Roine S, Viltanen M, Pöyhönen M, Baumann M. CADASIL: The most common hereditary subcortical vascular dementia Future Neurology. 3: 683-704. DOI: 10.2217/14796708.3.6.683 |
0.321 |
|
| 2007 |
Ihalainen S, Soliymani R, Iivanainen E, Mykkänen K, Sainio A, Pöyhönen M, Elenius K, Järveläinen H, Viitanen M, Kalimo H, Baumann M. Proteome analysis of cultivated vascular smooth muscle cells from a CADASIL patient. Molecular Medicine (Cambridge, Mass.). 13: 305-14. PMID 17622327 DOI: 10.2119/2006-00069.Ihalainen |
0.315 |
|
| 2007 |
Järvinen TA, Järvinen TL, Kääriäinen M, Aärimaa V, Vaittinen S, Kalimo H, Järvinen M. Muscle injuries: optimising recovery. Best Practice & Research. Clinical Rheumatology. 21: 317-31. PMID 17512485 DOI: 10.1016/J.Berh.2006.12.004 |
0.307 |
|
| 2007 |
Low WC, Junna M, Börjesson-Hanson A, Morris CM, Moss TH, Stevens DL, St Clair D, Mizuno T, Zhang WW, Mykkänen K, Wahlstrom J, Andersen O, Kalimo H, Viitanen M, Kalaria RN. Hereditary multi-infarct dementia of the Swedish type is a novel disorder different from NOTCH3 causing CADASIL. Brain : a Journal of Neurology. 130: 357-67. PMID 17235124 DOI: 10.1093/Brain/Awl360 |
0.302 |
|
| 2006 |
Miao Q, Paloneva T, Tuisku S, Roine S, Poyhonen M, Viitanen M, Kalimo H. Arterioles of the lenticular nucleus in CADASIL. Stroke; a Journal of Cerebral Circulation. 37: 2242-7. PMID 16873707 DOI: 10.1161/01.Str.0000236838.84150.C2 |
0.313 |
|
| 2006 |
Rostedt Punga A, Ahlqvist K, Bartoccioni E, Scuderi F, Marino M, Suomalainen A, Kalimo H, Stålberg EV. Neurophysiological and mitochondrial abnormalities in MuSK antibody seropositive myasthenia gravis compared to other immunological subtypes. Clinical Neurophysiology : Official Journal of the International Federation of Clinical Neurophysiology. 117: 1434-43. PMID 16737845 DOI: 10.1016/J.Clinph.2006.03.028 |
0.305 |
|
| 2005 |
Järvinen TA, Järvinen TL, Kääriäinen M, Kalimo H, Järvinen M. Muscle injuries: biology and treatment. The American Journal of Sports Medicine. 33: 745-64. PMID 15851777 DOI: 10.1177/0363546505274714 |
0.303 |
|
| 2004 |
Aärimaa V, Rantanen J, Best T, Schultz E, Corr D, Kalimo H. Mild eccentric stretch injury in skeletal muscle causes transient effects on tensile load and cell proliferation. Scandinavian Journal of Medicine & Science in Sports. 14: 367-72. PMID 15546332 DOI: 10.1111/J.1600-0838.2004.403.X |
0.332 |
|
| 2004 |
Aärimaa V, Kääriäinen M, Vaittinen S, Tanner J, Järvinen T, Best T, Kalimo H. Restoration of myofiber continuity after transection injury in the rat soleus. Neuromuscular Disorders : Nmd. 14: 421-8. PMID 15210165 DOI: 10.1016/J.Nmd.2004.03.009 |
0.303 |
|
| 2003 |
Järvinen TA, Józsa L, Kannus P, Järvinen TL, Hurme T, Kvist M, Pelto-Huikko M, Kalimo H, Järvinen M. Mechanical loading regulates the expression of tenascin-C in the myotendinous junction and tendon but does not induce de novo synthesis in the skeletal muscle. Journal of Cell Science. 116: 857-66. PMID 12571283 DOI: 10.1242/Jcs.00303 |
0.303 |
|
| 2002 |
Kääriäinen M, Nissinen L, Kaufman S, Sonnenberg A, Järvinen M, Heino J, Kalimo H. Expression of alpha7beta1 integrin splicing variants during skeletal muscle regeneration. The American Journal of Pathology. 161: 1023-31. PMID 12213731 DOI: 10.1016/S0002-9440(10)64263-0 |
0.321 |
|
| 2002 |
Kalimo H, Ruchoux MM, Viitanen M, Kalaria RN. CADASIL: a common form of hereditary arteriopathy causing brain infarcts and dementia. Brain Pathology (Zurich, Switzerland). 12: 371-84. PMID 12146805 DOI: 10.1111/J.1750-3639.2002.Tb00451.X |
0.333 |
|
| 2002 |
Kalaria RN, Kalimo H. Introduction: Non-atherosclerotic cerebrovascular disorders. Brain Pathology (Zurich, Switzerland). 12: 337-42. PMID 12146802 DOI: 10.1111/J.1750-3639.2002.Tb00448.X |
0.311 |
|
| 2002 |
Jääskeläinen SK, Juel VC, Udd B, Villanova M, Liguori R, Minassian BA, Falck B, Niemi P, Kalimo H. Electrophysiological findings in X-linked myopathy with excessive autophagy. Annals of Neurology. 51: 648-52. PMID 12112116 DOI: 10.1002/Ana.10173 |
0.314 |
|
| 2001 |
Tuominen S, Juvonen V, Amberla K, Jolma T, Rinne JO, Tuisku S, Kurki T, Marttila R, Pöyhönen M, Savontaus ML, Viitanen M, Kalimo H. Phenotype of a homozygous CADASIL patient in comparison to 9 age-matched heterozygous patients with the same R133C Notch3 mutation. Stroke; a Journal of Cerebral Circulation. 32: 1767-74. PMID 11486103 DOI: 10.1161/01.Str.32.8.1767 |
0.309 |
|
| 2001 |
Vaittinen S, Lukka R, Sahlgren C, Hurme T, Rantanen J, Lendahl U, Eriksson JE, Kalimo H. The expression of intermediate filament protein nestin as related to vimentin and desmin in regenerating skeletal muscle. Journal of Neuropathology and Experimental Neurology. 60: 588-97. PMID 11398835 DOI: 10.1093/Jnen/60.6.588 |
0.323 |
|
| 2001 |
Verkkoniemi A, Kalimo H, Paetau A, Somer M, Iwatsubo T, Hardy J, Haltia M. Variant Alzheimer disease with spastic paraparesis: neuropathological phenotype. Journal of Neuropathology and Experimental Neurology. 60: 483-92. PMID 11379823 DOI: 10.1093/Jnen/60.5.483 |
0.309 |
|
| 2000 |
Kääriäinen M, Järvinen T, Järvinen M, Rantanen J, Kalimo H. Relation between myofibers and connective tissue during muscle injury repair. Scandinavian Journal of Medicine & Science in Sports. 10: 332-7. PMID 11085560 DOI: 10.1034/J.1600-0838.2000.010006332.X |
0.321 |
|
| 2000 |
Houlden H, Baker M, McGowan E, Lewis P, Hutton M, Crook R, Wood NW, Kumar-Singh S, Geddes J, Swash M, Scaravilli F, Holton JL, Lashley T, Tomita T, Hashimoto T, ... ... Kalimo H, et al. Variant Alzheimer's disease with spastic paraparesis and cotton wool plaques is caused by PS-1 mutations that lead to exceptionally high amyloid-beta concentrations. Annals of Neurology. 48: 806-8. PMID 11079548 DOI: 10.1002/1531-8249(200011)48:5<806::Aid-Ana18>3.0.Co;2-F |
0.319 |
|
| 2000 |
Auranen M, Rapola J, Pihko H, Haltia M, Leivo I, Soinila S, Virtanen I, Kalimo H, Anderson LV, Santavuori P, Somer H. Muscle membrane-skeleton protein changes and histopathological characterization of muscle-eye-brain disease. Neuromuscular Disorders : Nmd. 10: 16-23. PMID 10677859 DOI: 10.1016/S0960-8966(99)00066-8 |
0.35 |
|
| 1999 |
Prihar G, Verkkoniem A, Perez-Tur J, Crook R, Lincoln S, Houlden H, Somer M, Paetau A, Kalimo H, Grover A, Myllykangas L, Hutton M, Hardy J, Haltia M. Alzheimer disease PS-1 exon 9 deletion defined. Nature Medicine. 5: 1090. PMID 10502791 DOI: 10.1038/13383 |
0.302 |
|
| 1999 |
Rantanen J, Hurme T, Kalimo H. Calf muscle atrophy and Achilles tendon healing following experimental tendon division and surgery in rats. Comparison of postoperative immobilization of the muscle-tendon complex in relaxed and tensioned positions. Scandinavian Journal of Medicine & Science in Sports. 9: 57-61. PMID 9974199 DOI: 10.1111/J.1600-0838.1999.Tb00208.X |
0.31 |
|
| 1999 |
Rantanen J, Thorsson O, Wollmer P, Hurme T, Kalimo H. Effects of therapeutic ultrasound on the regeneration of skeletal myofibers after experimental muscle injury. The American Journal of Sports Medicine. 27: 54-9. PMID 9934419 DOI: 10.1177/03635465990270011701 |
0.307 |
|
| 1998 |
Kääriäinen M, Kääriäinen J, Järvinen TL, Sievänen H, Kalimo H, Järvinen M. Correlation between biomechanical and structural changes during the regeneration of skeletal muscle after laceration injury. Journal of Orthopaedic Research : Official Publication of the Orthopaedic Research Society. 16: 197-206. PMID 9621894 DOI: 10.1002/Jor.1100160207 |
0.319 |
|
| 1998 |
Thorsson O, Rantanen J, Hurme T, Kalimo H. Effects of nonsteroidal antiinflammatory medication on satellite cell proliferation during muscle regeneration. The American Journal of Sports Medicine. 26: 172-6. PMID 9548108 DOI: 10.1177/03635465980260020401 |
0.322 |
|
| 1998 |
Panula P, Rinne J, Kuokkanen K, Eriksson KS, Sallmen T, Kalimo H, Relja M. Neuronal histamine deficit in Alzheimer's disease. Neuroscience. 82: 993-7. PMID 9466423 DOI: 10.1016/S0306-4522(97)00353-9 |
0.309 |
|
| 1997 |
Udd B, Krahe R, Wallgren-Pettersson C, Falck B, Kalimo H. Proximal myotonic dystrophy--a family with autosomal dominant muscular dystrophy, cataracts, hearing loss and hypogonadism: heterogeneity of proximal myotonic syndromes? Neuromuscular Disorders : Nmd. 7: 217-28. PMID 9196902 DOI: 10.1016/S0960-8966(97)00041-2 |
0.324 |
|
| 1996 |
Oksi J, Kalimo H, Marttila RJ, Marjamäki M, Sonninen P, Nikoskelainen J, Viljanen MK. Inflammatory brain changes in Lyme borreliosis. A report on three patients and review of literature. Brain : a Journal of Neurology. 119: 2143-54. PMID 9010017 DOI: 10.1093/Brain/119.6.2143 |
0.304 |
|
| 1996 |
Valtonen M, Näntö-Salonen K, Heinänen K, Alanen A, Kalimo H, Simell O. Skeletal muscle of patients with gyrate atrophy of the choroid and retina and hyperornithinaemia in ultralow-field magnetic resonance imaging and computed tomography. Journal of Inherited Metabolic Disease. 19: 729-34. PMID 8982944 DOI: 10.1007/Bf01799162 |
0.314 |
|
| 1996 |
Tyni T, Majander A, Kalimo H, Rapola J, Pihko H. Pathology of skeletal muscle and impaired respiratory chain function in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency with the G1528C mutation. Neuromuscular Disorders : Nmd. 6: 327-37. PMID 8938697 DOI: 10.1016/0960-8966(96)00352-5 |
0.315 |
|
| 1995 |
Rantanen J, Ranne J, Hurme T, Kalimo H. Denervated segments of injured skeletal muscle fibers are reinnervated by newly formed neuromuscular junctions. Journal of Neuropathology and Experimental Neurology. 54: 188-94. PMID 7876887 DOI: 10.1097/00005072-199503000-00005 |
0.313 |
|
| 1995 |
Rissanen A, Kalimo H, Alaranta H. Effect of intensive training on the isokinetic strength and structure of lumbar muscles in patients with chronic low back pain. Spine. 20: 333-40. PMID 7732470 DOI: 10.1097/00007632-199502000-00014 |
0.302 |
|
| 1994 |
Kalimo H, Sourander P, Järvi O, Hakola P. Vascular changes and blood-brain barrier damage in the pathogenesis of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy (membranous lipodystrophy). Acta Neurologica Scandinavica. 89: 353-61. PMID 8085433 DOI: 10.1111/J.1600-0404.1994.Tb02646.X |
0.3 |
|
| 1993 |
Udd B, Partanen J, Halonen P, Falck B, Hakamies L, Heikkilä H, Ingo S, Kalimo H, Kääriäinen H, Laulumaa V. Tibial muscular dystrophy. Late adult-onset distal myopathy in 66 Finnish patients. Archives of Neurology. 50: 604-8. PMID 8503797 DOI: 10.1001/Archneur.1993.00540060044015 |
0.349 |
|
| 1993 |
Rantanen J, Hurme M, Falck B, Alaranta H, Nykvist F, Lehto M, Einola S, Kalimo H. The lumbar multifidus muscle five years after surgery for a lumbar intervertebral disc herniation. Spine. 18: 568-74. PMID 8484147 DOI: 10.1097/00007632-199304000-00008 |
0.307 |
|
| 1992 |
Laurikainen E, Aitasalo K, Halonen P, Falck B, Kalimo H. Muscle pathology in idiopathic cricopharyngeal dysphagia. Enzyme histochemical and electron microscopic findings. European Archives of Oto-Rhino-Laryngology : Official Journal of the European Federation of Oto-Rhino-Laryngological Societies (Eufos) : Affiliated With the German Society For Oto-Rhino-Laryngology - Head and Neck Surgery. 249: 216-23. PMID 1386521 DOI: 10.1007/Bf00178473 |
0.335 |
|
| 1992 |
Hurme T, Kalimo H. Adhesion in skeletal muscle during regeneration. Muscle & Nerve. 15: 482-9. PMID 1373471 DOI: 10.1002/Mus.880150412 |
0.319 |
|
| 1991 |
Hurme T, Lehto M, Falck B, Tainio H, Kalimo H. Electromyography and morphology during regeneration of muscle injury in rats. Acta Physiologica Scandinavica. 142: 443-56. PMID 1950596 DOI: 10.1111/J.1748-1716.1991.Tb09179.X |
0.31 |
|
| 1991 |
Hurme T, Kalimo H, Lehto M, Järvinen M. Healing of skeletal muscle injury: an ultrastructural and immunohistochemical study. Medicine and Science in Sports and Exercise. 23: 801-10. PMID 1921672 DOI: 10.1249/00005768-199107000-00006 |
0.319 |
|
| 1991 |
Kallajoki M, Hyypiä T, Halonen P, Orvell C, Rima BK, Kalimo H. Inclusion body myositis and paramyxoviruses. Human Pathology. 22: 29-32. PMID 1845865 DOI: 10.1016/0046-8177(91)90057-V |
0.309 |
|
| 1990 |
Michelsson JE, Aho HJ, Kalimo H, Haltia M. Severe degeneration of rabbit vastus intermedius muscle immobilized in shortened position. Apmis : Acta Pathologica, Microbiologica, Et Immunologica Scandinavica. 98: 336-44. PMID 2354053 DOI: 10.1111/J.1699-0463.1990.Tb01041.X |
0.326 |
|
| 1989 |
Lehto M, Hurme M, Alaranta H, Einola S, Falck B, Järvinen M, Kalimo H, Mattila M, Paljärvi L. Connective tissue changes of the multifidus muscle in patients with lumbar disc herniation. An immunohistologic study of collagen types I and III and fibronectin. Spine. 14: 302-9. PMID 2711245 DOI: 10.1097/00007632-198903000-00010 |
0.314 |
|
| 1989 |
Kalimo H, Rantanen J, Viljanen T, Einola S. Lumbar muscles: structure and function. Annals of Medicine. 21: 353-9. PMID 2532525 DOI: 10.3109/07853898909149220 |
0.309 |
|
| 1988 |
Conradi NG, Kalimo H, Sourander P. Reactions of vessel walls and brain parenchyma to the accumulation of Gaucher cells in the Norrbottnian type (type III) of Gaucher disease. Acta Neuropathologica. 75: 385-90. PMID 3364161 DOI: 10.1007/Bf00687792 |
0.31 |
|
| 1988 |
Salahuddin TS, Johansson BB, Kalimo H, Olsson Y. Structural changes in the rat brain after carotid infusions of hyperosmolar solutions. An electron microscopic study. Acta Neuropathologica. 77: 5-13. PMID 3149121 DOI: 10.1007/Bf00688236 |
0.302 |
|
| 1987 |
Paljärvi L, Kalimo H, Lang H, Savontaus ML, Sonninen V. Minicore myopathy with dominant inheritance. Journal of the Neurological Sciences. 77: 11-22. PMID 3806134 DOI: 10.1016/0022-510X(87)90202-4 |
0.346 |
|
| 1986 |
Mattila M, Hurme M, Alaranta H, Paljärvi L, Kalimo H, Falck B, Lehto M, Einola S, Järvinen M. The multifidus muscle in patients with lumbar disc herniation. A histochemical and morphometric analysis of intraoperative biopsies. Spine. 11: 732-8. PMID 3787345 DOI: 10.1097/00007632-198609000-00013 |
0.319 |
|
| 1984 |
Paljärvi L, Karjalainen K, Kalimo H. Altered muscle saccharide pattern in X-linked muscular dystrophy. Archives of Neurology. 41: 39-42. PMID 6689886 DOI: 10.1001/Archneur.1984.04050130045020 |
0.314 |
|
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