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1. 若年性皮膚筋炎および多発性筋炎：疫学、病因および臨床症状juvenile dermatomyositis and polymyositis epidemiology pathogenesis and clinical manifestations [show details]
… Juvenile dermatomyositis (JDM) and juvenile polymyositis (JPM) are rare autoimmune myopathies in childhood. JDM is primarily a capillary vasculopathy, whereas JPM involves direct T cell invasion of muscle …
2. 若年性皮膚筋炎および多発性筋炎：診断juvenile dermatomyositis and polymyositis diagnosis [show details]
… Juvenile dermatomyositis (JDM) and juvenile polymyositis (JPM) are rare autoimmune myopathies affecting children. JDM is characterized primarily as a capillary vasculopathy, whereas JPM involves direct …
3. 若年性皮膚筋炎および多発性筋炎：治療、合併症および予後juvenile dermatomyositis and polymyositis treatment complications and prognosis [show details]
… Juvenile dermatomyositis (JDM) and juvenile polymyositis (JPM) are autoimmune myopathies of childhood. JDM is primarily a capillary vasculopathy, whereas JPM involves direct T cell invasion of muscle …
4. 思春期に生じる多嚢胞性卵巣症候群の診断的評価diagnostic evaluation of polycystic ovary syndrome in adolescents [show details]
… Young Women Health of Boston Children Hospital ; – From the Pediatric Endocrine Society (PES) and the American Academy of Pediatrics (AAP) Links to society… normal testosterone levels fall 10 percent from 8 AM to 4 PM and double during midcycle .…
5. 学会が公開する診療ガイドラインのリンク：皮膚筋炎・多発性筋炎society guideline links dermatomyositis and polymyositis [show details]
… and major clinical response in adult dermatomyositis and polymyositis – An International Myositis Assessment and Clinical… Hub and Access point for pediatric Rheumatology in Europe (SHARE): Consensus-based recommendations for the management of juvenile dermatomyositis (2017) …

English Journal

Juvenile global tremor: a clinicopathologic syndrome mimicking polymyoclonia.

Melick NR, Chutorian A, Miller DC.
Pediatric neurology. 2007 Oct;37(4)280-2.
Olivary nucleus degeneration is one of the pathologic characteristics of infantile olivopontocerebellar atrophy. It has also been described in premature neonates and infants with severe perinatal asphyxia and is thought to represent retrograde transsynaptic changes from cerebellar hemisphere lesions
PMID 17903673

Long-term observation of the changing brainstem auditory evoked potentials in a case of infantile opsoclonus-polymyoclonia syndrome.

Horikawa M, Ohtaki E, Urabe F, Kawano Y, Amamoto M, Matsuishi T.
Brain & development. ;15(4)308-10.
Brainstem auditory evoked potential (BAEP) studies were repeatedly carried out on a boy with infantile opsoclonus-polymyoclonia syndrome, from 15 months to 39 months of age, the following being revealed: the I-III interpeak latency (I-III IPL) was more or less in the upper normal range until 24 mont
PMID 8250156

High-dose i.v. human immunoglobulin in a case with infantile opsoclonus polymyoclonia syndrome.

Sugie H, Sugie Y, Akimoto H, Endo K, Shirai M, Ito M.
Acta paediatrica (Oslo, Norway : 1992). 1992 Apr;81(4)371-2.
We report a 14-month-old male with infantile opsoclonus polymyoclonia syndrome. His clinical disabilities responded favorably to high-dose human immunoglobulin therapy. High dose immunoglobulin therapy is one of the therapies for patients with this syndrome.
PMID 1606405