Search

Your search keyword '"Oka, Akira"' showing total 34 results

Search Constraints

Start Over You searched for: Author "Oka, Akira" Remove constraint Author: "Oka, Akira" Publisher elsevier Remove constraint Publisher: elsevier
34 results on '"Oka, Akira"'

Search Results

1. Adrenocorticotropic hormone therapy alters Q-albumin ratios in patients with infantile epileptic spasms syndrome of unknown etiology.

2. Assessment of patients' characteristics associated with the efficacy and safety of oral valganciclovir treatment for infants with symptomatic congenital cytomegalovirus disease.

3. Long-term analysis of adrenocorticotropic hormone monotherapy for infantile epileptic spasms syndrome with periventricular leukomalacia.

4. Fetal heart rate evolution and brain imaging findings in preterm infants with severe cerebral palsy.

5. Lectin-Like Oxidized Low-Density Lipoprotein Receptor-1-Related Microglial Activation in Neonatal Hypoxic-Ischemic Encephalopathy: Morphologic Consideration.

6. Epidemiological changes of acute encephalopathy in Japan based on national surveillance for 2014-2017.

7. Case-control association study of rare nonsynonymous variants of SCN1A and KCNQ2 in acute encephalopathy with biphasic seizures and late reduced diffusion.

8. Thermolabile polymorphism of carnitine palmitoyltransferase 2: A genetic risk factor of overall acute encephalopathy.

9. RXRB Is an MHC-Encoded Susceptibility Gene Associated with Anti-Topoisomerase I Antibody-Positive Systemic Sclerosis.

10. Genome-wide association study for mandibular prognathism using microsatellite and pooled DNA method.

11. Brain edema with clasmatodendrosis complicating ataxia telangiectasia.

12. Perinatal dioxin exposure and psychosocial and behavioral development in school-aged children.

13. Holoprosencephaly with cerebellar vermis hypoplasia in 13q deletion syndrome: Critical region for cerebellar dysgenesis within 13q32.2q34.

14. Organic cation transporter/solute carrier family 22a is involved in drug transfer into milk in mice.

15. Epithelial protein lost in neoplasm modulates platelet-derived growth factor-mediated adhesion and motility of mesangial cells.

16. Microsatellite genome-wide association study for mandibular prognathism.

17. LOX-1 is a novel therapeutic target in neonatal hypoxic-ischemic encephalopathy.

18. Polymorphisms in TLR-2 are associated with congenital cytomegalovirus (CMV) infection but not with congenital CMV disease.

19. Alu-mediated nonallelic homologous and nonhomologous recombination in the BMPR2 gene in heritable pulmonary arterial hypertension.

20. Single nucleotide polymorphisms and outcome risk in unrelated mismatched hematopoietic stem cell transplantation: an exploration study.

21. Epidemiology of acute encephalopathy in Japan, with emphasis on the association of viruses and syndromes.

22. A novel splicing variant of CADM2 as a protective transcript of psoriasis.

23. Meta-analysis confirms the LCE3C_LCE3B deletion as a risk factor for psoriasis in several ethnic groups and finds interaction with HLA-Cw6.

24. Interstitial deletion of 13q14.13-q32.3 presenting with Arima syndrome and bilateral retinoblastoma.

25. Comprehensive genetic analyses of PLP1 in patients with Pelizaeus-Merzbacher disease applied by array-CGH and fiber-FISH analyses identified new mutations and variable sizes of duplications.

26. Cortical gray matter lesions in acute encephalopathy with febrile convulsive status epilepticus.

27. A novel POMT2 mutation causes mild congenital muscular dystrophy with normal brain MRI.

28. Infantile neuronal ceroid lipofuscinosis: the first reported case in Japan diagnosed by palmitoyl-protein thioesterase enzyme activity deficiency.

29. Mental retardation, spasticity, basal ganglia calcification, cerebral white matter lesions, multiple endocrine defects, telangiectasia and atrophic skin: a new syndrome?

30. Behavioral and psychiatric disorders in Prader-Willi syndrome: a population study in Japan.

31. Alternative splicing due to an intronic SNP in HMSD generates a novel minor histocompatibility antigen.

32. Fukutin expression in mouse non-muscle somatic organs: its relationship to the hypoglycosylation of alpha-dystroglycan in Fukuyama-type congenital muscular dystrophy.

33. Molecular genetic study in Japanese patients with Alexander disease: a novel mutation, R79L.

34. Unilateral occlusion of the middle cerebral artery after varicella-zoster virus infection.

Catalog

Books, media, physical & digital resources