Intravenous gammaglobulin therapy of Satoyoshi syndrome
スポンサーリンク
概要
著者
-
MAEKAWA Kihei
Department of Pediatrics,Jikei University School of Medicine
-
Nara Takahiro
Division Of Neurology Saitama Children's Medical Center
-
Nara Takahiro
Division Of Neurology Saitama Chidren's Medical Center
-
Maekawa Kihei
Department Of Pediatrics Jikei University School Of Medicine
-
ARITA Jiro
Division of Neurology, Saitama Chidren's Medical Center
-
HAMANO Shin-ichiro
Division of Neurology, Saitama Chidren's Medical Center
-
Nara Takahiro
Division Of Child And Reproductive Health Course Of Health Science Graduate School Of Medicine Osaka
-
Arita Jiro
Division Of Neurology Saitama Chidren's Medical Center
-
Maekawa Kihei
Department Of Liberal Art And Human Development University Of Human Service
-
Hamano Shin-ichiro
Division Of Neurology Saitama Chidren's Medical Center
関連論文
- Early intervention for very-low-birth-weight infants
- Intravenous gammaglobulin therapy of Satoyoshi syndrome
- Ex vivo expansion of umbilical cord blood hematopoietic progenitor cells by combinations of cytokines
- Effects of cytokines on hematopoietic progenitor cells in cord blood, in bone marrow, and in peripheral blood mobilized by chemotherapy and G-CSF
- Morphometric development of the human fetal auditory system: inferior collicula nucleus
- A JAPANESE PATIENT WITH X-LINKED α-THALASSEMIA/MENTAL RETARDATION SYNDROME : AN ADDITIONAL CASE REPORT
- Founders of child neurology in Japan - Kihei Maekawa
- Long-term follow up of abdominal aortic aneurysm complicating Kawasaki disease : Comparison of ethe ffectiveness of different imaging methods
- CT screening for unrecognized coronary sequal of Kawasaki disease
- Postnatal evolution of cortical malformation in the "non-affected" hemisphere of hemimegalencephaly
- The axonal damage marker tau protein in the cerebrospinal fluid is increased in patients with acute encephalopathy with biphasic seizures and late reduced diffusion
- Paroxysmal kinesigenic choreoathetosis associated with prenatal brain damage
- Clinical and genetic studies of five fatal cases of Japanese Gaucher disease type 1
- Simultaneous assay of prostaglandins and thromboxane in the cerebrospinal fluid by gas chromatography-mass spectrometry-selected ion monitoring
- Syndrome of microcephaly, Dandy-Walker malformation, and Wilms tumor caused by mosaic variegated aneuploidy with premature centromere division (PCD) : report of a new case and review of the literature
- Early infantile manifestations of incontinentia pigmenti mimicking acute encephalopathy
- Acute autonomic sensory and motor neuropathy associated with parvovirus B19 infection
- Effectiveness and safety of non-intravenous high-dose phenobarbital therapy for intractable epilepsy during childhood