Haruki Koike

Summary

Affiliation: Nagoya University
Country: Japan

Publications

  1. doi request reprint Impact of aging on the progression of neuropathy after liver transplantation in transthyretin Val30Met amyloidosis
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    Muscle Nerve 46:964-70. 2012
  2. doi request reprint The spectrum of immune-mediated autonomic neuropathies: insights from the clinicopathological features
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    J Neurol Neurosurg Psychiatry 84:98-106. 2013
  3. doi request reprint The spectrum of clinicopathological features in pure autonomic neuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, 466 8550, Japan
    J Neurol 259:2067-75. 2012
  4. doi request reprint Late-onset familial amyloid polyneuropathy in Japan
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Amyloid 19:55-7. 2012
  5. doi request reprint Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai Cho, Showa Ku, Nagoya 466 8550, Japan
    J Neurol Neurosurg Psychiatry 83:152-8. 2012
  6. doi request reprint Systemic but asymptomatic transthyretin amyloidosis 8 years after domino liver transplantation
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    J Neurol Neurosurg Psychiatry 82:1287-90. 2011
  7. doi request reprint Electrophysiological features of late-onset transthyretin Met30 familial amyloid polyneuropathy unrelated to endemic foci
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, 466 8550, Japan
    J Neurol 255:1526-33. 2008
  8. doi request reprint Distinct characteristics of amyloid deposits in early- and late-onset transthyretin Val30Met familial amyloid polyneuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    J Neurol Sci 287:178-84. 2009
  9. doi request reprint The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Aichi, Japan
    Amyloid 16:142-8. 2009
  10. doi request reprint IgM MGUS anti-MAG neuropathy with predominant muscle weakness and extensive muscle atrophy
    Yuichi Kawagashira
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Muscle Nerve 42:433-5. 2010

Collaborators

Detail Information

Publications54

  1. doi request reprint Impact of aging on the progression of neuropathy after liver transplantation in transthyretin Val30Met amyloidosis
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    Muscle Nerve 46:964-70. 2012
    ..Information related to the long-term follow-up of neuropathy in patients with familial amyloid polyneuropathy after liver transplantation is still scarce...
  2. doi request reprint The spectrum of immune-mediated autonomic neuropathies: insights from the clinicopathological features
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    J Neurol Neurosurg Psychiatry 84:98-106. 2013
    ..An overlap with autoimmune autonomic ganglionopathy has been suggested in these settings...
  3. doi request reprint The spectrum of clinicopathological features in pure autonomic neuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, 466 8550, Japan
    J Neurol 259:2067-75. 2012
    ..05). In conclusion, the clinical and pathological features of pure autonomic neuropathy vary in terms of progression, autonomic involvement, presence of the antiganglionic acetylcholine receptor antibody, and loss of unmyelinated fibers...
  4. doi request reprint Late-onset familial amyloid polyneuropathy in Japan
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Amyloid 19:55-7. 2012
    ..The causal mechanism of differences between the early- and late-onset forms of FAP with the same mutation in the TTR gene has not yet been determined...
  5. doi request reprint Natural history of transthyretin Val30Met familial amyloid polyneuropathy: analysis of late-onset cases from non-endemic areas
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai Cho, Showa Ku, Nagoya 466 8550, Japan
    J Neurol Neurosurg Psychiatry 83:152-8. 2012
    ..The objective of this study was to elucidate the natural history of late-onset transthyretin Val30Met-associated familial amyloid polyneuropathy (FAP ATTR Val30Met) in non-endemic areas...
  6. doi request reprint Systemic but asymptomatic transthyretin amyloidosis 8 years after domino liver transplantation
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    J Neurol Neurosurg Psychiatry 82:1287-90. 2011
    ..This case allows for the characterisation of amyloid deposition during the asymptomatic stage of FAP. Widespread amyloid deposition may occur before tissue damage in this disease...
  7. doi request reprint Electrophysiological features of late-onset transthyretin Met30 familial amyloid polyneuropathy unrelated to endemic foci
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, 466 8550, Japan
    J Neurol 255:1526-33. 2008
    ..Through the development of gene diagnostic techniques, late-onset transthyretin Met30-associated familial amyloid polyneuropathy (FAP TTR Met30) has been shown to be more prevalent than is generally believed...
  8. doi request reprint Distinct characteristics of amyloid deposits in early- and late-onset transthyretin Val30Met familial amyloid polyneuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    J Neurol Sci 287:178-84. 2009
    ..Amyloid deposition in late-onset cases may be similar to that observed in senile systemic amyloidosis with wild-type TTR deposition, suggesting that aging may play an important role in these cases...
  9. doi request reprint The significance of carpal tunnel syndrome in transthyretin Val30Met familial amyloid polyneuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Aichi, Japan
    Amyloid 16:142-8. 2009
    ..The electrophysiological abnormality at the distal portion of the median nerve may be a consequence of polyneuropathy rather than an entrapment injury...
  10. doi request reprint IgM MGUS anti-MAG neuropathy with predominant muscle weakness and extensive muscle atrophy
    Yuichi Kawagashira
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Muscle Nerve 42:433-5. 2010
    ..Sural nerve biopsy revealed widely spaced myelin and positive staining of myelinated fibers with an IgM antibody. Predominant motor symptoms with muscle atrophy can be one of the clinical manifestations of anti-MAG neuropathy...
  11. doi request reprint Intravenous immunoglobulin treatment for painful sensory neuropathy associated with Sjögren's syndrome
    Saori Morozumi
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    J Neurol Sci 279:57-61. 2009
    ..Patients with painful sensory neuropathy associated with Sjögren's syndrome-associated neuropathy often show severe neuropathic pain which is not relieved by conventional treatments...
  12. doi request reprint Differential, size-dependent sensory neuron involvement in the painful and ataxic forms of primary Sjögren's syndrome-associated neuropathy
    Yuichi Kawagashira
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    J Neurol Sci 319:139-46. 2012
    ..This hypothesis may have an impact on therapeutic approach...
  13. doi request reprint Rapidly developing weakness mimicking Guillain-Barré syndrome in beriberi neuropathy: two case reports
    Haruki Koike
    Department of Neurology, Nagoya University School of Medicine, Nagoya, Japan
    Nutrition 24:776-80. 2008
    ..We examined the diagnostic difficulty in thiamine deficiency...
  14. ncbi request reprint Clinicopathologic and genetic features of early- and late-onset FAP type I (FAP ATTR Val30Met) in Japan
    Gen Sobue
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    Amyloid 10:32-8. 2003
    ..Unmyelinated fibers in the biopsied sural nerve specimens of late-onset cases seemed to be relatively well preserved compared to those of previously reported early-onset cases...
  15. doi request reprint Morphological progression of myelin abnormalities in IgM-monoclonal gammopathy of undetermined significance anti-myelin-associated glycoprotein neuropathy
    Yuichi Kawagashira
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    J Neuropathol Exp Neurol 69:1143-57. 2010
    ..Loosening of compact myelin seems to contribute to tomacula formation...
  16. doi request reprint Spatial distribution of nerve fiber pathology and vasculitis in microscopic polyangiitis-associated neuropathy
    Saori Morozumi
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    J Neuropathol Exp Neurol 70:340-8. 2011
    ....
  17. doi request reprint Clinicopathological features of acute autonomic and sensory neuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Brain 133:2881-96. 2010
    ..Small neuronal cells in the autonomic and sensory ganglia may be affected in the initial phase, and subsequently, large neuronal cells in the sensory ganglia are damaged...
  18. ncbi request reprint The wide spectrum of clinical manifestations in Sjögren's syndrome-associated neuropathy
    Keiko Mori
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Brain 128:2518-34. 2005
    ....
  19. ncbi request reprint Demyelinating and axonal features of Charcot-Marie-Tooth disease with mutations of myelin-related proteins (PMP22, MPZ and Cx32): a clinicopathological study of 205 Japanese patients
    Naoki Hattori
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Brain 126:134-51. 2003
    ....
  20. ncbi request reprint Nonmyelinating Schwann cell involvement with well-preserved unmyelinated axons in Charcot-Marie-Tooth disease type 1A
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    J Neuropathol Exp Neurol 66:1027-36. 2007
    ..In conclusion, there is marked alteration of the population and morphology of nonmyelinating Schwann cells, and axon-Schwann cell interactions seem to be regulated differently between myelinated and unmyelinated fibers in CMT1A...
  21. ncbi request reprint Myopathy in thiamine deficiency: analysis of a case
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    J Neurol Sci 249:175-9. 2006
    ..Tenderness in the limb muscles has been reported anecdotally in patients with beriberi neuropathy, but clinical effects of thiamine deficiency on skeletal muscle have received little attention...
  22. doi request reprint IgG4-related neuropathy: a case report
    Ken Ohyama
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    JAMA Neurol 70:502-5. 2013
    ..We describe, for the first time, the clinical features and nerve biopsy findings of a patient with IgG4-RD who presented with neuropathy in the extremities...
  23. doi request reprint Diagnosis of sporadic transthyretin Val30Met familial amyloid polyneuropathy: a practical analysis
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Japan
    Amyloid 18:53-62. 2011
    ..Detecting subclinical cardiac involvement may help to diagnose late-onset FAP ATTR Val30Met in those without a family history of the disease...
  24. ncbi request reprint Type I (transthyretin Met30) familial amyloid polyneuropathy in Japan: early- vs late-onset form
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Japan
    Arch Neurol 59:1771-6. 2002
    ..We have also reported late-onset Japanese cases unrelated to an endemic focus and showing distinctive clinicopathologic features...
  25. doi request reprint A novel MPZ mutation in Charcot-Marie-Tooth disease type 1B with focally folded myelin and multiple entrapment neuropathies
    Madoka Iida
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Neuromuscul Disord 22:166-9. 2012
    ..A sural nerve biopsy performed at age 49 revealed focally folded myelin. Molecular genetic analysis revealed a novel Asn131Ser mutation in MPZ...
  26. doi request reprint Differential response to intravenous immunoglobulin (IVIg) therapy among multifocal and polyneuropathy types of painful diabetic neuropathy
    Yuichi Kawagashira
    Department of Neurology, Nagoya University Graduate School of Medicine, 65 Tsurumai Cho, Showa Ku, Nagoya 466 8550, Japan
    J Clin Neurosci 17:1003-8. 2010
    ..Pain associated with diabetic neuropathy is multifactorial and causative factors are heterogeneous. Our results show that IVIg therapy can alleviate pain in patients with multifocal diabetic neuropathy...
  27. ncbi request reprint Alcoholic neuropathy is clinicopathologically distinct from thiamine-deficiency neuropathy
    Haruki Koike
    Department of Neurology, Nagoya University, Graduate School of Medicine, Nagoya, Japan
    Ann Neurol 54:19-29. 2003
    ..However, features of alcoholic neuropathy is influenced by concomitant thiamine-deficiency state, having so far caused the obscure clinicopathological entity of alcoholic neuropathy...
  28. ncbi request reprint Identification of novel sequence variants in the neurofilament-light gene in a Japanese population: analysis of Charcot-Marie-Tooth disease patients and normal individuals
    Tsuyoshi Yoshihara
    Department of Neurology, Nagoya University Graduate School of Medicine, Japan
    J Peripher Nerv Syst 7:221-4. 2002
    ..The variant alleles in the NF-L gene could influence the developing process of CMT phenotype and also might cause CMT phenotype...
  29. doi request reprint Autonomic manifestations in acute sensory ataxic neuropathy: a case report
    Ken Ohyama
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Auton Neurosci 179:155-8. 2013
    ..Additionally, the pupillary response to pilocarpine revealed the presence of parasympathetic dysfunction. In conclusion, widespread, subclinical autonomic dysfunctions may be present in ASAN patients. ..
  30. doi request reprint Clinicopathological features of neuropathy associated with lymphoma
    Minoru Tomita
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Brain 136:2563-78. 2013
    ....
  31. doi request reprint The significance of folate deficiency in alcoholic and nutritional neuropathies: analysis of a case
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Nutrition 28:821-4. 2012
    ..To elucidate the significance of folate deficiency in alcoholic and nutritional neuropathies...
  32. ncbi request reprint The wide range of clinical manifestations in leprous neuropathy: two case reports
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Japan
    Intern Med 50:2223-6. 2011
    ..These cases highlight the fact that, as a result of worldwide travel and immigration, leprosy should still be considered in the differential diagnosis of neuropathy in developed countries...
  33. ncbi request reprint Postgastrectomy polyneuropathy with thiamine deficiency is identical to beriberi neuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Nutrition 20:961-6. 2004
    ..We assessed whether postgastrectomy polyneuropathy associated with thiamine deficiency is clinicopathologically identical to beriberi neuropathy, including a biochemical determination of thiamine status...
  34. doi request reprint Acute superficial sensory neuropathy with generalized anhidrosis, anosmia, and ageusia
    Yu Miyazaki
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya 466 8550, Japan
    Muscle Nerve 43:286-8. 2011
    ..The impaired pain and temperature sensation remained distributed along cranial and spinal dermatomes in a non-length-dependent manner, suggesting that the ganglionopathy affected small neurons...
  35. ncbi request reprint [Metabolic and nutritional neuropathy]
    Naoki Hattori
    Department of Neurology, Nagoya University Graduate School of Medicine
    Rinsho Shinkeigaku 48:1026-7. 2008
    ..However, features of alcoholic neuropathy is influenced by concomitant thiamine-deficiency state, having so far caused the obscure clinicopathological entity of alcoholic neuropathy...
  36. ncbi request reprint Demographic features of Japanese patients with sporadic inclusion body myositis: a single-center referral experience
    Hirotaka Nakanishi
    Department of Neurology, Nagoya University Graduate School of Medicine, Japan
    Intern Med 52:333-7. 2013
    ..The aim of this study was to clarify the demographic features of Japanese patients with sIBM...
  37. ncbi request reprint Demyelinating neuropathy and autoimmune hemolytic anemia in a patient with pancreatic cancer
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Japan
    Intern Med 52:1737-40. 2013
    ..Although the combination of AIHA and CIDP has been reported anecdotally, this is the first case of the coexistence of these diseases as paraneoplastic syndromes. ..
  38. doi request reprint Spinal cord stimulation markedly ameliorated refractory neuropathic pain in transthyretin Val30Met familial amyloid polyneuropathy
    Yu Miyazaki
    Department of Neurology, Nagoya University Graduate School of Medicine, Japan
    Amyloid 18:87-90. 2011
    ....
  39. ncbi request reprint Differential recovery in cardiac and vasomotor sympathetic functional markers in a patient with acute autonomic sensory and motor neuropathy
    Ken Ohyama
    Department of Neurology, Nagoya Daini Red Cross Hospital, Japan
    Intern Med 52:497-502. 2013
    ..However, orthostatic hypotension was prolonged. These results suggest a differential improvement in the cardiac and vasomotor sympathetic functions...
  40. pmc Hypophosphataemic neuropathy in a patient who received intravenous hyperalimentation
    Yohei Iguchi
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    J Neurol Neurosurg Psychiatry 78:1159-60. 2007
  41. doi request reprint Paraneoplastic neuropathy: wide-ranging clinicopathological manifestations
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Curr Opin Neurol 24:504-10. 2011
    ..The goal of this article was to review the recent literature describing the wide-ranging clinicopathological manifestations of paraneoplastic neuropathy...
  42. doi request reprint Polymorphism of transient axonal glycoprotein-1 in chronic inflammatory demyelinating polyneuropathy
    Masahiro Iijima
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    J Peripher Nerv Syst 16:52-5. 2011
    ..In conclusion, SNPs in TAG-1, which is a key molecule for axon-Schwann cell interactions and is distributed at the juxtaparanode, are related to the IVIg responsiveness of CIDP patients...
  43. ncbi request reprint [Therapeutic strategy for CIDP (chronic inflammatory demyelinating polyneuropathy)]
    Masahiro Iijima
    Department of Neurology, Nagoya University Graduate School of Medicine
    Nihon Rinsho 71:855-60. 2013
    ..Further study of FLTs is required, such as whether a combination of IVIg and corticosteroids is reasonable as an induced therapy for CIDP...
  44. ncbi request reprint [Efficacy and availability of intravenous immunoglobulin in chronic inflammatory demyelinating polyneuropathy]
    Masahiro Iijima
    Department of Neurology, Nagoya University Graduate School of Medicine
    Nihon Rinsho 70:715-21. 2012
    ..Those cytokines may be controlled by sialylated Fc in the immunoglobulin preparation. These findings may be followed by the development of more efficient and reasonable IVIg preparations...
  45. ncbi request reprint Alcoholic neuropathy
    Haruki Koike
    Department of Neurology, Nagoya University, Graduate School of Medicine, Nagoya, Japan
    Curr Opin Neurol 19:481-6. 2006
    ..We describe clinicopathologic features of alcoholic neuropathy, taking the effect of thiamine status into consideration, and recent progress associated with the pathogenesis...
  46. doi request reprint Clinicopathological features of neuropathy in anti-neutrophil cytoplasmic antibody-associated vasculitis
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, 466 8550, Japan
    Clin Exp Nephrol 17:683-5. 2013
    ..Hence, CSS- and MPA-associated neuropathies share common neuropathic features, but the extent of systemic organ involvement is significantly higher in MPA cases, resulting in poorer survival rates. ..
  47. doi request reprint Effect of age and sex differences on wild-type transthyretin amyloid formation in familial amyloidotic polyneuropathy: a proteomic approach
    Masayoshi Tasaki
    Department of Neurology, Graduate School of Medical Sciences, Kumamoto University, 1 1 1 Honjo, Kumamoto 860 0811, Japan Department of Immunology and Hematology, Division of Informative Clinical Science, Graduate School of Medical Sciences, Kumamoto University, 4 24 1 Kuhonji, Kumamoto 862 0976, Japan
    Int J Cardiol 170:69-74. 2013
    ..To elucidate age and sex differences in FAP, we investigated biochemical characteristics of amyloid deposits in different tissue sites of FAP by proteomic analysis...
  48. ncbi request reprint [Sjogren's syndrome-associated neuropathy]
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine
    Brain Nerve 65:1333-42. 2013
    ..In conclusion, the clinicopathological features of neuropathies associated with Sjogren's syndrome are highly variable. The neuropathy classification is important from a therapeutic point of view...
  49. ncbi request reprint [Autoimmune autonomic ganglionopathy and acute autonomic and sensory neuropathy]
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine
    Rinsho Shinkeigaku 53:1326-9. 2013
    ..Hence, small neurons in the autonomic and sensory ganglia may be affected in the initial phase and, subsequently, large neurons in the sensory ganglia are damaged in acute autonomic and sensory neuropathy. ..
  50. ncbi request reprint Neuronal intranuclear inclusion disease cases with leukoencephalopathy diagnosed via skin biopsy
    Jun Sone
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Aichi, Japan
    J Neurol Neurosurg Psychiatry . 2013
  51. doi request reprint Paraneoplastic neuropathy
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine, Nagoya, Japan
    Handb Clin Neurol 115:713-26. 2013
    ..Recognition and diagnosis of paraneoplastic neuropathy is important, as neuropathic symptoms usually precede the identification of the primary tumor, and treatment at an earlier stage provides better chances of good outcomes. ..
  52. doi request reprint Diagnosis of familial amyloid polyneuropathy: wide-ranged clinicopathological features
    Haruki Koike
    Nagoya University Graduate School of Medicine, Department of Neurology, Nagoya 466 8550, Japan 81 52 744 2385 81 52 744 2384
    Expert Opin Med Diagn 4:323-31. 2010
    ....
  53. ncbi request reprint Mortality and morbidity in peripheral neuropathy associated Churg-Strauss syndrome and microscopic polyangiitis
    Naoki Hattori
    Department of Neurology, Nagoya University School of Medicine, Japan
    J Rheumatol 29:1408-14. 2002
    ..We investigated whether the neuropathy in these 2 diseases reveals differences in clinicopathologic features and predicts survival and functional outcome...
  54. ncbi request reprint [Clinicopathological features of familial amyloid polyneuropathy]
    Haruki Koike
    Department of Neurology, Nagoya University Graduate School of Medicine
    Rinsho Shinkeigaku 51:1134-7. 2011
    ..Therefore, tight recognition for the possibility of FAP ATTR Val30Met are needed at the time of initial evaluation of neuropathy of undetermined etiology to avoid missed diagnosis...