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English Journal

Congenital thrombotic thrombocytopenic purpura: Upshaw-Schulman syndrome: a cause of neonatal death and review of literature.

Sharma D1, Shastri S2, Pandita A3, Sharma P4.
The journal of maternal-fetal & neonatal medicine : the official journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians.J Matern Fetal Neonatal Med.2016 Jun;29(12):1977-9. doi: 10.3109/14767058.2015.1071789. Epub 2015 Sep 12.
Thrombotic thrombocytopenic purpura (TTP) is a rare disorder in children characterized by microangiopathic hemolytic anemia (MAHA) and thrombocytopenia. The classic Moschcowitz Pentads of TTP include hemolytic anemia, with fragmentation of erythrocytes, thrombocytopenia, diffuse and non-focal neurol
PMID 26365135

History, Epidemiology, and Clinical Manifestations of Zika: A Systematic Review.

Paixão ES1, Barreto F1, da Glória Teixeira M1, da Conceição N Costa M1, Rodrigues LC1.
American journal of public health.Am J Public Health.2016 Apr;106(4):606-12. doi: 10.2105/AJPH.2016.303112.
OBJECTIVES: To describe salient epidemiological characteristics of Zika virus outbreaks across the world and to examine the clinical presentations, complications, and atypical manifestations related to their occurrence in recent history.METHODS: We conducted a systematic review of the literature by
PMID 26959260

Proposal for electrodiagnostic evaluation of patients with suspected ulnar neuropathy at the elbow.

Omejec G1, Podnar S2.
Clinical neurophysiology : official journal of the International Federation of Clinical Neurophysiology.Clin Neurophysiol.2016 Apr;127(4):1961-7. doi: 10.1016/j.clinph.2016.01.011. Epub 2016 Jan 28.
OBJECTIVE: To develop an evidence-based electrodiagnostic (EDx) approach to patients with suspected ulnar neuropathy at the elbow (UNE).METHODS: We prospectively recruited patients with suspected UNE, took a history and performed clinical neurologic, EDx and ultrasonographic (US) examinations. Ulnar
PMID 26971477

ミトコンドリアDNA 8729 G>A変異をみとめたneurogenic muscle weakness, ataxia, and retinitis pigmentosa（NARP）の1例

宮脇統子,古東秀介,石原広之,後藤雄一,西野一三,苅田典生,戸田達史
臨床神経学 55(2), 91-95, 2015
症例は31歳の女性である．小児期より長距離走が不得意で，23歳より易転倒，31歳より歩行時のふらつきが増悪し受診した．神経学的に小脳失調，下肢優位の四肢筋力低下，腱反射低下，振動覚低下，ミオクローヌス，感音性難聴，網膜色素変性症をみとめた．MRIで小脳脳幹の萎縮があり，血清・髄液中の乳酸・ピルビン酸が高値，針筋電図検査で慢性神経原性変化をみとめた．生検筋の組織検査ではragged-red fibe …
NAID 130004921307

大野慶子,木村百合香
耳鼻咽喉科臨床 108(2), 133-138, 2015
… An 83-year-old man presented to the emergency department of our hospital with disorder of consciousness (Japan coma scale I-2), weakness of the limbs, and a 4-day history of neck pain. … Based on the literature and our experience, we believe that although rare, spinal epidural abscesses are a critical complication that could result in a severe decline in neurologic function or death if diagnosis and treatment are delayed. …
NAID 130004827510