Atypical X-linked Agammaglobulinemia Diagnosed in Three Adult

スポンサーリンク

概要

著者

関連論文

ブルトン・チロシン・キナーゼの第1イントロンにおける転写調節異常
Characterization of Ventricular Myocardial Performance in the Fetus by Tissue Doppler Imaging
正常健常児において左室内血流伝搬速度に影響を与える要因の検討
Open Heart Operation in a Child With Congenital Heart Disease and Hereditary Spherocytosis
Genetic Analysis in Patients with Left Ventricular Noncompaction and Evidence for Genetic Heterogeneity(Myocardial Disease, Cardiomyopathy and Myocarditis (M), The 69th Annual Scientific Meeting of the Japanese Circulation Society)
OJ-273 Validation of Myocardial Acceleration during Isovolumic Contraction as a Noninvasive Index of Left Ventricular Contractility(Echo/Doppler 10 (I) : OJ32)(Oral Presentation (Japanese))
OE-283 Profound S100A12 Expression in Neutrophils in Early Stage of Acute Kawasaki Disease(Congenital Heart Disease/Kawasaki's Disease 1 (M) : OE35)(Oral Presentation (English))
Clinical features of isolated left ventricular noncompaction : infantile type and juvenile type
Hepatocyte growth factor in transient myeloproliferative disorder of Down syndrome
Distinct Clones Are Associated with the Development of Transient Myeloproliferative Disorder and Acute Megakaryocytic Leukemia in a Patient with Down Syndrome
OE-269 Evidence of Genetic Heterogeneity in Left Ventricular Noncompaction(Cardiomyopathy, basic/clinical-1 (M) OE45,Oral Presentation (English),The 70th Anniversary Annual Scientific Meeting of the Japanese Circulation Society)
Outcome of Non-T-Cell-Depleted HLA-Haploidentical Hematopoietic Stem Cell Transplantation from Family Donors in Children and Adolescents
Clinical and Genetic Analyses of Presumed Shwachman-Diamond Syndrome in Japan
Evans syndrome in a patient with Langerhans cell histiocytosis : possible pathogenesis of autoimmunity in LCH
Early lineage switch in an infant acute lymphoblastic leukemia
Successful Cardiac Resynchronization Therapy in a 3-Year-Old Girl With Isolated Left Ventricular Non-Compaction and Narrow QRS Complex : A Case Report
Pneumocystis jiroveci pneumonia as an atypical presentation of X-linked agammaglobulinemia
Spontaneous regression of aleukemic leukemia cutis harboring a NPM/RARA fusion gene in an infant with cutaneous mastosytosis
Molecular characterization of two novel VEGFR3 mutations in Japanese families with Milroy's disease
PE-306 SCN5A Variant in Japanese Patients with Left Ventricular Noncompaction and Arrhythmia(Cardiomyopathy, basic/clinical-4, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
Acute lymphoblastic leukemia after living donor liver transplantation
Mutational Analysis of the WASP Gene in 2 Korean Families with Wiskott-Aldrich Syndrome
Identification of mutations in the Bruton's tyrosine kinase gene, including a novel genomic rearrangements resulting in large deletion, in Korean X-linked agammaglobulinemia patients
von Recklinghausen Disease in a Patient with X-linked Agammaglobulinemia
Non-Hodgkin's Lymphoma of the Ascending Colon in a Patient with Becker Muscular Dystrophy : Report of a Case
Orally Active GPIIb/IIIa Antagonists : Synthesis and Biological Activities of Masked Amidines as Prodrugs of 2-[(3S)-4-[(2S)-2-(4-Amidinobenzoylamino)-3-(4-methoxyphenyl)propanoyl]-3-(2-methoxy-2-oxoethyl)-2-oxopiperazinyl]acetic Acid
Novel Non-Peptide GPIIb/IIIa Antagonists : Synthesis and Biological Activities of 2-[4-[2-(4-Amidinobenzoylamino)-2-(substituted)acetyl]-3-(2-methoxy-2-oxoethyl)-2-oxopiperazinyl]acetic Acids
A Patient with Acromegaly Who Showed Remarkable Improvement of Hyperglycemia after Treatment with Octreotide
Atypical X-linked Agammaglobulinemia Diagnosed in Three Adult
Characterization of a Novel Nonsense Mutation in the Interleukin-7 Receptor α Gene in a Korean Patient with Severe Combined Immunodeficiency
Point mutation in intron 11 of Bruton's tyrosine kinase in atypical X-linked agammaglobulinemia
A novel immunoregulatory protein in human colostrum, syntenin-1, for promoting the development of IgA-producing cells from cord blood B cells
von Recklinghausen Disease in a Patient with X-linked Agammaglobulinemia
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
Autoimmune lymphoproliferative syndrome mimicking chronic active Epstein-Barr virus infection
Atypical case of X-linked agammaglobulinemia diagnosed at 45 years of age
Hematopoietic stem cell transplantation with reduced intensity conditioning from a family haploidentical donor in an infant with familial hemophagocytic lymphohistocytosis
Genetic analysis of contiguous X-chromosome deletion syndrome encompassing the BTK and TIMM8A genes
Delayed onset adenosine deaminase deficiency associated with acute disseminated encephalomyelitis

もっと見る

スポンサーリンク