Shinji Saitoh
Saitoh, Saburou, 1944-
![Sudoc [ABES], France](/viaf/images/flags/SUDOC.png "Sudoc [ABES], France")
Saitoh, Saburou
Saitoh, Saburu
斎藤, 三郎, 1944-
Saitoh, S. (1944- ).
齋藤, 三郎
VIAF ID: 110002232 (Personal)
Permalink: http://viaf.org/viaf/110002232
Preferred Forms
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100 1 _ ‡a Saitoh, S. ‡d (1944- ).
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100 1 _ ‡a Saitoh, Saburou
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100 1 _ ‡a Saitoh, Saburou
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100 1 _ ‡a Saitoh, Saburou ‡d (1944- )
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100 1 _
‡a
Saitoh, Saburou
‡d
1944-
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100 1 _
‡a
Saitoh, Saburou,
‡d
1944-
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100 1 _ ‡a Saitoh, Saburou, ‡d 1944-
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100 1 _
‡a
Saitoh, Saburou,
‡d
1944-
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100 1 _ ‡a Saitoh, Saburou, ‡d 1944-
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100 1 _
‡a
Saitoh, Saburu
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100 0 _
‡a
Shinji Saitoh
-
100 1 _
‡a
斎藤, 三郎,
‡d
1944-
-
100 1 _
‡a
齋藤, 三郎
4xx's: Alternate Name Forms (22)
5xx's: Related Names (3)
Works
| Title | Sources |
|---|---|
| Analytic extension formulas and their applications |
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| The identification of two pathogenic variants in a family with mild and severe forms of developmental delay |
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| Impaired neuronal KCC2 function by biallelic SLC12A5 mutations in migrating focal seizures and severe developmental delay |
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| Imprint switching on human chromosome 15 may involve alternative transcripts of the SNRPN gene |
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| Increased protein stability of CDKN1C causes a gain-of-function phenotype in patients with IMAGe syndrome |
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| Inflammatory changes in infantile-onset LMNA-associated myopathy |
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| Inflammatory cytokine tumor necrosis factor α suppresses neuroprotective endogenous erythropoietin from astrocytes mediated by hypoxia-inducible factor-2α. |
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| Integrative Analyses of De Novo Mutations Provide Deeper Biological Insights into Autism Spectrum Disorder. |
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| Intrauterine growth and the maturation process of adrenal function |
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| Kaisekigaku ni okeru mondai no keisanki ni yoru kaihō |
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| Kenkyūsha sōran, shizen, 1984: |
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| KIF1A mutation in a patient with progressive neurodegeneration |
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| Macitentan reverses early obstructive pulmonary vasculopathy in rats: early intervention in overcoming the survivin-mediated resistance to apoptosis. |
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| Magnetoencephalographic analysis of paroxysmal fast activity in patients with epileptic spasms |
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| Magnetoencephalography localizing spike sources of atypical benign partial epilepsy |
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| MEG time-frequency analyses for pre- and post-surgical evaluation of patients with epileptic rhythmic fast activity |
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| MERRF/MELAS overlap syndrome: a double pathogenic mutation in mitochondrial tRNA genes |
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| Minimal definition of the imprinting center and fixation of chromosome 15q11-q13 epigenotype by imprinting mutations. |
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| Molecular dissection of the Prader-Willi/Angelman syndrome region (15q11-13) by YAC cloning and FISH analysis |
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| Molecular genetic analysis of 30 families with Joubert syndrome |
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| Molecular genetic and clinical delineation of 22 patients with congenital hypogonadotropic hypogonadism |
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| Molecular Genetic Dissection and Neonatal/Infantile Intrahepatic Cholestasis Using Targeted Next-Generation Sequencing |
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| Mosaic paternally derived inv dup(15) may partially rescue the Prader-Willi syndrome phenotype with uniparental disomy |
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| Mutations in COG2 encoding a subunit of the conserved oligomeric golgi complex cause a congenital disorder of glycosylation |
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| Mutations of the FHL1 gene cause Emery-Dreifuss muscular dystrophy |
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| New convolutions and norm inequalities |
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| Non-skewed X-inactivation may cause mental retardation in a female carrier of X-linked alpha-thalassemia/mental retardation syndrome (ATR-X): X-inactivation study of nine female carriers of ATR-X. |
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| Novel DCX mutation-caused lissencephaly in a boy and very mild heterotopia in his mother. |
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| Novel MCA/ID syndrome with ASH1L mutation |
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| Novel splicing mutation in the ASXL3 gene causing Bainbridge-Ropers syndrome |
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| Parent-of-origin specific histone acetylation and reactivation of a key imprinted gene locus in Prader-Willi syndrome. |
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| Parthenogenetic chimaerism/mosaicism with a Silver-Russell syndrome-like phenotype. |
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| Perinatal management of neonatal alloimmune thrombocytopenia associated with anti-group A antibody |
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| Peripartum depression and infant care, sleep and growth |
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| Pharmacoresistant epileptic eyelid twitching in a child with a mutation in SYNGAP1. |
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| Phenotype variability and allelic heterogeneity in KMT2B-Associated disease. |
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| Phenotypic spectrum of COL4A1 mutations: porencephaly to schizencephaly |
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| Pitfall in the Diagnosis of Fructose-1,6-Bisphosphatase Deficiency: Difficulty in Detecting Glycerol-3-Phosphate with Solvent Extraction in Urinary GC/MS Analysis |
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| Possible involvement of the tip of temporal lobe in Landau-Kleffner syndrome |
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| Predominant area of brain lesions in neonates with herpes simplex encephalitis |
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| Prenatal diagnosis of X-linked recessive Lenz microphthalmia syndrome |
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| Primary microcephaly with anterior predominant pachygyria caused by novel compound heterozygous mutations in ASPM. |
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| Probability curves for predicting symptom severity during oral food challenge with milk |
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| Publisher Correction: IMSindel: An accurate intermediate-size indel detection tool incorporating de novo assembly and gapped global-local alignment with split read analysis |
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| Radial Glial Fibers Promote Neuronal Migration and Functional Recovery after Neonatal Brain Injury. |
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| Refined generalizations of the triangle inequality on Banach spaces |
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| Regional Differences in Clinical Features of Kaposiform Hemangioendothelioma of the Intestinal Tract |
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| Respiratory illness and acute flaccid myelitis in the Tokai district in 2018 |
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| Rikōkei bibun hōteishiki no kaihō |
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| Rikōkei fukuso kaiseki |
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| Role of a heterotrimeric G-protein, Gi2, in the corticogenesis: possible involvement in periventricular nodular heterotopia and intellectual disability |
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| Saiseikaku no riron nyūmon |
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| Schaaf-Yang syndrome shows a Prader-Willi syndrome-like phenotype during infancy |
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| Siblings with optic neuropathy and RTN4IP1 mutation |
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| Single nucleotide polymorphisms inAGTR1,TFAP2B, andTRAF1are not associated with the incidence of patent ductus arteriosus in Japanese preterm infants |
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| SNP array screening of cryptic genomic imbalances in 450 Japanese subjects with intellectual disability and multiple congenital anomalies previously negative for large rearrangements. |
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| Solution methods by computers in analysis |
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| Successful alternative treatment containing vindesine for acute lymphoblastic leukemia with Charcot-Marie-Tooth disease |
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| Successful cochlear implantation in a patient with mitochondrial hearing loss and m.625G>A transition |
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| Survival of fetuses with severe oligohydramnios |
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| Targeted next-generation sequencing in the diagnosis of neurodevelopmental disorders |
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| Temple syndrome: comprehensive molecular and clinical findings in 32 Japanese patients. |
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| Thalamic lesions in acute encephalopathy with biphasic seizures and late reduced diffusion |
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| Theory of reproducing kernels and its applications |
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| Tissue-limited ring chromosome 18 mosaicism as a cause of Pitt-Hopkins syndrome |
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| Treatment Strategy for Pediatric Paratesticular Rhabdomyosarcoma Based on Chimeric Gene Assessment |
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| TUBA1A mutation can cause a hydranencephaly-like severe form of cortical dysgenesis |
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| Uniparental disomy and imprinting defects in Japanese patients with Angelman syndrome |
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| Unmasking 15q12 deletion using microarray-based comparative genomic hybridization in a mentally retarded boy with r(Y) |
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| Vaccine-associated paralytic poliomyelitis in a non-immunocompromised infant |
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| Visualization of the spatial positioning of the SNRPN, UBE3A, and GABRB3 genes in the normal human nucleus by three-color 3D fluorescence in situ hybridization |
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| West syndrome associated with mosaic duplication ofFOXG1in a patient with maternal uniparental disomy of chromosome 14 |
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| Wide clinical variability in a family with a CACNA1A T666m mutation: hemiplegic migraine, coma, and progressive ataxia |
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| A woman with 46,XX,dup(16)(p13.11 p13.3) and the ATR-X phenotype. |
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| Yoakemae : Yotchan no omoi |
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| 夜明け前 : よっちゃんの想い |
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| 再生核の応用についての総合的な研究 |
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| 再生核の理論入門 |
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| 理工系複素解析 |
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| 理工系微分方程式の解法 |
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| 解析学における問題の計算機による解法 |
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