Search Results - "Masuko, Kaori"

  • Showing 1 - 10 results of 10
Refine Results
  1. 1

    Laryngeal dystonia in xeroderma pigmentosum by Muto, Ayako, Matsui, Akira, Saito, Yoshiaki, Iwamoto, Hiroko, Kaneko, Kaori, Masuko, Kaori, Chikumaru, Yuri, Saito, Kazuyo, Kimura, Seiji

    Published in Brain & development (Tokyo. 1979) (01-12-2005)
    “…We report on three patients with xeroderma pigmentosum group A (XPA) who showed laryngeal stridor in their 20s. The stridor appeared on feeding and emotional…”
    Get full text
    Journal Article
  2. 2

    Brain MRI findings of older patients with Pallister–Killian syndrome by Saito, Yoshiaki, Masuko, Kaori, Kaneko, Kaori, Chikumaru, Yuri, Saito, Kazuyo, Iwamoto, Hiroko, Matsui, Akira, Aida, Noriko, Kurosawa, Kenji, Kuroki, Yoshikazu, Kimura, Seiji

    Published in Brain & development (Tokyo. 1979) (2006)
    “…Pallister–Killian syndrome (PKS) is a disorder caused by a mosaic tetrasomy of chromosome 12p, which manifests with dysmorphism, intellectual disabilities,…”
    Get full text
    Journal Article
  3. 3

    Two cases of acute disseminated encephalomyelitis which occurred before the age of 24 months by Tanoue, Koji, Yamashita, Sumimasa, Masuko, Kaori, Osaka, Jin, Iai, Mizue, Yamada, Michiko

    Published in No to hattatsu (01-09-2006)
    “…We report two female cases of acute disseminated encephalomyelitis with onset of 19 and 15 months, respectively. MRI demonstrated the T2-high lesions in the…”
    Get more information
    Journal Article
  4. 4

    Disturbed respiratory cycle accompanying hypoxic-ischemic encephalopathy by Saito, Yoshiaki, Masuko, Kaori, Kaneko, Kaori, Saito, Kazuyo, Chikumaru, Yuri, Iwamoto, Hiroko, Matsui, Akira, Kimura, Seiji

    Published in No to hattatsu (01-09-2005)
    “…We report the case of a 2-year-old boy who experienced total asphyxia at 4 months of age, and suffered abnormalities at specific phases of the respiratory…”
    Get more information
    Journal Article
  5. 5

    A case of long-term survival of a patient with infantile Alexander disease diagnosed by DNA analysis by Wakabayashi, Kazuyo, Lai, Mizue, Masuko, Kaori, Yamashita, Sumimasa, Yamada, Michiko, Iwamoto, Hiroko, Aida, Noriko, Shiroma, Naohide, Kanazawa, Naomi, Tsujino, Seiichi

    Published in No to hattatsu (01-01-2005)
    “…Alexander disease is a hereditary disorder of myelin degeneration. The pathological feature of the brain is the characteristic inclusion bodies in astrocytes…”
    Get more information
    Journal Article
  6. 6
  7. 7
  8. 8

    SPECT and Localized Proton MRS of Epilepsy in Children with Cortical Dysplasia by Matsuzawa, Junko, Konishi, Tohru, Masuko, Kaori, Hongou, Kazuhisa, Yamatani, Miwa, Yagi, Shinichi, Miyawaki, Toshio

    Published in Epilepsia (Copenhagen) (01-05-1998)
    “…Purpose: Recently cortical dysplasia (CD) attracted attention because of its importance as a focus for epilepsy and a lesion for surgery. However, the clinical…”
    Get full text
    Journal Article
  9. 9
  10. 10

    Flunitrazepam for sleep disturbance in children with intractable epilepsy by Konishi, Tohru, Masuko, Kaori, Naganuma, Yoshihiro, Hongou, Kazuhisa, Yagi, Shinichi

    Published in Brain & development (Tokyo. 1979) (1995)
    “…Add-on therapy with flunitrazepam (FNZ) was performed in 5 children with marked sleep disturbance and intractable seizures. Correction of the sleep disturbance…”
    Get full text
    Journal Article