Juvenile myelomonocytic leukemia presenting multiple painful erythematous lesions diagnosed as Sweet's syndrome
スポンサーリンク
概要
- 論文の詳細を見る
- 2008-06-01
著者
-
ITO Etsuro
Department of Pediatrics, Hirosaki University School of Medicine
-
Ito E
Department Of Pediatrics Hirosaki University School Of Medicine
-
Kitamura Hideo
Department of Dermatology, Hirosaki University Graduate School of Medicine
-
Nakano Hajime
Department of Dermatology, Hirosaki University Graduate School of Medicine
-
Ito Eturo
弘前大学 医学部皮膚科学
-
SAWAMURA Daisuke
Department of Dermatology, School of Medicine, Hirosaki University Hirosaki
-
TERUI KIMINORI
Department of Pediatrics, Hirosaki University School of Medicine
-
Terui Kiminori
Department Of Pediatrics Hirosaki University School Of Medicine
-
Sawamura Daisuke
駿河台日本大学病院 皮膚科
-
Sawamura Daisuke
Department Of Dermatology Hirosaki University Graduate School Of Medicine
-
KANEKO Takahide
Department of Dermatology, Hirosaki University School of Medicine
-
Nakano H
Department Of Dermatology Hirosaki University Graduate School Of Medicine
-
Nakano Hajime
弘前大学 医学部皮膚科学
-
Nakano Hajime
駿河台日本大学病院 皮膚科
-
Kimura Hiroto
Department Of Dermatology Hirosaki University School Of Medicine
-
Nakano Hajime
Department Of Dermatology Hirosaki University Graduate School Of Medicine
-
Kitamura Hideo
Department Of Dermatology Hirosaki University School Of Medicine
-
Kaneko Takahide
Department Of Dermatology Hirosaki University Graduate School Of Medicine
-
Ito Etsuro
Department Of Pediatrics Hirosaki University Graduate School Of Medicine
-
Terui Kiminori
Department Of Pediatrics Hirosaki University Graduate School Of Medicine
-
Nakano Hajime
Department Of Cardiovascular Medicine Ohmori Hospital Toho University School Of Medicine
-
Sawamura Daisuke
Department of Dermatology, Hirosaki University School of Medicine
関連論文
- Dense deposit disease presenting as endocapillary proliferative nephritis
- Characterization of Hair Follicles in Hirosaki Hairless Rats with Deletion of Basic Hair Keratin Genes. Enlarged Medulla, Loss of Cuticle and Long Catagen
- Retinoic acid-inducible gene-I（ RIG-I） and diseases
- Renal Biopsy Findings in Children Receiving Long-Term Treatment with Cyclosporine A Given as a Single Daily Dose
- Effective Treatment with Cyclosporine A of a Child with Systemic Lupus Erythematosus Resistant to Cyclophosphamide Pulse Therapy
- Mizoribine Pulse Therapy for a Pediatric Patient with Steroid-Resistant Nephrotic Syndrome
- Effective Therapy of a Child Case of Refractory Nephrotic Syndrome with Tacrolimus
- Combined therapy of enalapril and losartan attenuates histologic progression in immunoglobulin A nephropathy
- Therapy-related membranous nephropathy in juvenile idiopathic arthritis with Turner syndrome
- Mizoribine oral pulse therapy for a patient with severe lupus nephritis
- End-Stage Kidney at the Onset of Nephrotic Syndrome in a 4-Year-Old Girl
- Acute renal failure due to hypertension : Malignant hypertension in an adolescent
- Disseminated candidiasis following prednisolone therapy in systemic lupus erythematosus
- Tubulointerstitial Nephritis and Uveitis Syndrome in Two Siblings
- Three novel mutations of the fibrillin-1 gene and ten single nucleotide polymorphisms of the fibrillin-3 gene in Marfan syndrome patients
- Role of β-defensins in oral epithelial health and disease
- Cloning and Characterization of the Novel Chimeric Gene p53/FXR2 in the Acute Megakaryoblastic Leukemia Cell Line CMK11-5
- Expression of Transcription Factors during Megakaryocytic Differentiation of CD34^+ Cells from Human Cord Blood Induced by Thrombopoietin
- Progression from myelodysplastic syndrome with monosomy 7 to acute monoblastic leukemia with MLL gene rearrangement
- Successful Outcome of Mismatched Hematopoietic Stem Cell Transplantation from a Related Donor in an Infant with Acute Lymphoblastic Leukemia and 9 ; 11 Translocation : Case Report and Review of the Literature
- Hemolytic crisis with fulminant hepatic failure in Wilson disease without consanguinity
- Low serum lipids suggest severe bone marrow failure in children with aplastic anemia
- Sporadic case of hemoglobin Bushwick detected by chance in aplastic crisis
- Fatal Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis With Clonal Karyotype Abnormality
- Risk of Etoposide-Related Acute Myeloid Leukemia in the Treatment of Epstein-Barr Virus-Associated Hemophagocytic Lymphohistiocytosis
- Hepatocyte growth factor in transient myeloproliferative disorder of Down syndrome
- The Promoter of Mouse Transcription Repressor bach1 Is Regulated by Sp1 and Trans-Activated by Bach^1
- Distinct Clones Are Associated with the Development of Transient Myeloproliferative Disorder and Acute Megakaryocytic Leukemia in a Patient with Down Syndrome
- Conserved Structure, Regulatory Elements, and Transcriptional Regulation from the GATA-1 Gene Testis Promoter^1
- -473-IS PTCA EFFECTIVE STRATEGY FOR SILENT MYOCARDIAL ISCHEMIA (SMI)? : EFFICACY OF PTCA FOR SMI IN TERMS OF ANAEROBIC THRESHOLD (AT) : PTCA, CABG : FREE COMMUNICATIONS(II) : PROCEEDINGS OF THE 53th ANNUAL SCIENTIFIC MEETING OF THE JAPANESE CIRCULATION SO
- Amicrobial pustulosis associated with IgA nephropathy and Sjögren's syndrome
- ITGB4 missense mutation in a transmembrane domain causes non-lethal variant of junctional epidermolysis bullosa with pyloric atresia
- Keratin 1 Gene Mutation Detected in Epidermal Nevus with Epidermolytic Hyperkeratosis
- Compound heterozygous mutations including a de novo missense mutation in ABCA12 led to a case of harlequin ichthyosis with moderate clinical severity
- Juvenile myelomonocytic leukemia presenting multiple painful erythematous lesions diagnosed as Sweet's syndrome
- COL7A1 mutation G2037E causes epidermal retention of type VII collagen
- In vivo transfer of TGF-α and β genes to keratinocytes
- Low-grade myxofibrosarcoma invaded into the underlying skeletal muscle
- Remodeling of desmosomal and hemidesmosomal adhesion systems during human hair follicle development
- Cytokine modulation of retinoic acid-inducible gene-I (RIG-I) expression in human epidermal keratinocytes
- Genetic Analysis of Shwachman-Diamond Syndrome : Phenotypic Heterogeneity in Patients Carrying Identical SBDS Mutations
- Semiempirical Calculations of Force Constants for Torsional and Stretching Vibrations in Excited States of Retinal and Its Related Compounds
- Possible role of 1,25-dihydroxyvitamin D_3-induced metallothionein in photoprotection against UVB injury in mouse skin and cultured rat keratinocytes
- A Japanese family with dominant pretibial dystrophic epidermolysis bullosa : Identification of a new glycine substitution in the triple-helical collagenous domain of type VII collagen
- Genotype-phenotype correlation in non-Hallopeau-Siemens recessive dystrophic epidermolysis bullosa : The splice site mutation c.6216+5G>T in the COL7A1 gene results in aberrant and normal splicings
- A case of Meckel's diverticulum adherent to the posterior abdominal wall : the efficacy of small-bowel radiography coupled with barium enema examination
- PJ-480 A Study of Characteristics of Myocardial Bridge in Patients with Myocardial Infarction by Using Multi-Detector Computed Tomography(PJ081,CT/MRI (Coronary/Vascular) 3 (I),Poster Session (Japanese),The 73rd Annual Scientific Meeting of The Japanese C
- PJ-665 Evaluation of Myocardial Bridge and its Proximal Regions on MDCT(CT / DSA(10)(I),Poster Session(Japanese),The 72nd Annual Scientific Meeting of the Japanese Circulation Society)
- PJ-798 Comparison between Long-acting and Short-acting Loop Diuretics in Chronic Heart Failure : Evaluation by I123MIBG(Heart failure, clinical-18, The 71st Annual Scientific Meeting of the Japanese Circulation Society)
- OJ-134 The effect of varsaltan on insulin resistance and Aortic stiffness in hypertensive patients(Atherosclerosis, Clinical 2 (IHD) : OJ16)(Oral Presentation (Japanese))
- Effect of Helicobacter pylori eradication in the treatment of Japanese patients with chronic idiopathic urticaria
- Novel p.M1T and recurrent p.G301S mutations in cathepsin C in a Japanese patient with Papillon-Lefevre syndrome : Implications for understanding the genotype/phenotype relationship
- A novel homozygous missense mutation in the fatty aldehyde dehydrogenase gene causes Sjogren-Larsson syndrome
- Dominant dystrophic epidermolysis bullosa caused by a novel G2037R mutation and by a known G2028R mutation in the type VII collagen gene (COL7A1)
- A novel Sp1-family-related cis-acting element for transcription of type VII collagen gene (COL7A1)
- Expression vector with DNA of bovine papilloma virus 1 for keratinocyte gene therapy
- A KERATIN K10 GENE MUTATION IN A JAPANESE PATIENT WITH EPIDERMOLYTIC HYPERKERATOSIS
- Clinical and genetic analysis of Fabry disease : report of six cases including three heterozygous females
- Novel mutation in a fumalate hydratase gene of a Japanese patient with multiple cutaneous and uterine leiomyomatosis
- Improved Survival of Children with Advanced Neuroblastoma Treated by Intensified Therapy Including Myeloablative Chemotherapy with Stem Cell Transplantation : A Retrospective Analysis from the Tohoku Neuroblastoma Study Group
- Decrease in Thy-1 Expression on Peripheral CD34 Positive Cells Induced by G-CSF Mobilization
- Recurrent erythroblastopenia associated with Varicella zoster virus infection in an infant
- Calcineurin/NFAT-dependent regulation of 230-kDa bullous pemphigoid antigen (BPAG1) gene expression in normal human epidermal keratinocytes
- Significance of sentinel node biopsy in the management of squamous cell carcinoma arising from recessive dystrophic epidermolysis bullosa
- Vitamin D_3 inhibits expression of bullous pemphigoid antigen 1 through posttranscriptional mechanism without new protein synthesis
- A method for rapid evaluation of photoaging by measuring fluorescence intensity of green fluorescent protein due to elastin promoter activity
- Human Metallothionein Gene Expression Is Upregulated by β-Thujaplicin : Possible Involvement of Protein Kinase C and Reactive Oxygen Species(Molecular and Cell Biology)
- A case of bullous dermatitis artefacta possibly induced by a deodorant spray
- A Japanese Case of Nuchal-Type Fibroma
- A Case of Photocontact Urticaria Induced by Photodynamic Therapy with Topical 5-Aminolaevulinic Acid
- Superficial Granulomatous Pyoderma : A Case Report of Two Japanese Patients and Clinical Comparison with Foreign Patients
- Bach1 Deficiency Ameliorates Hepatic Injury in a Mouse Model
- Subsequent Progression to Membranous Glomerulonephritis Following Exacerbation of Urticarial Rash in Systemic Lupus Erythematosus : Report of 2 Cases
- A unique monoclonal antibody 29A stains the cytoplasm of amniotic epithelia and cutaneous basement membrane
- Possible role of endoplasmic reticulum stress in the pathogenesis of Darier's disease
- Tyrosinase gene analysis in Japanese patients with oculocutaneous albinism
- Genetic studies of 20 Japanese families of dystrophic epidermolysis bullosa
- The G2028R glycine substitution mutation in COL7A1 leads to marked inter-familiar clinical heterogeneity in dominant dystrophic epidermolysis bullosa
- Theory of Retinal and Its Related Compounds by the Extended INDO-CI Method Taking Account of the Change in Bond Lengths in Consistence with Electronic States
- Semiempirical Calculation of Force Constants of Stretching Vibrations in Excited States of Retinal and Its Related Compounds
- Coexistence of Generalized Morphea with Histological Changes in Lichen Sclerosus et Atrophicus and Lichen Planus
- Benefits of Once-Daily Administration of Cyclosporine A for Children with Steroid-Dependent, Relapsing Nephrotic Syndrome
- Depigmented Macula as an Initial Manifestation of Extramammary Paget's Disease
- Linear immunoglobulin A bullous dermatosis possibly induced by mefenamic acid
- Leukemia cutis is an early sign of blast transformation that may mimic a common skin disease : Sycosis-like eruptions in chronic myelomonocytic leukemia
- Selective KIT inhibitor KI-328 and HSP90 inhibitor show different potency against the type of KIT mutations recurrently identified in acute myeloid leukemia
- Relation between the expression levels of the POU transcription factors Skn-1a and Skn-1n and keratinocyte differentiation
- Raf kinase inhibitor protein expression correlates with differentiation but not with ERK phosphorylation in cutaneous squamous cell carcinoma
- Lymphoscintigraphy for sentinel lymph node mapping in Japanese patients with malignant skin neoplasms of the lower extremities : comparison with previously investigated Japanese lymphatic anatomy
- Overview of epidermolysis bullosa
- Hailey-Hailey disease with affective disorder : Report of a case with novel ATP2C1 gene mutation
- Dystrophic epidermolysis bullosa pruriginosa of elderly onset
- Expression of Raf Kinase Inhibitor Protein in Keratinocyte Differentiation in the Mouse Epidermis
- Garlic-induced irritant contact dermatitis mimicking nail psoriasis
- The compound heterozygote for new/recurrent COL7A1 mutations in a Japanese patient with bullous dermolysis of the newborn
- Successful Multidrug Treatment of a Pediatric Patient with Severe Churg-Strauss Syndrome Refractory to Prednisolone
- Two cases of recessive dystrophic epidermolysis bullosa diagnosed as severe generalized
- Characterization of Stimulator of Interferon Genes (STING) Expression in Human Epidermal Keratinocytes
- Reduction in epidermal Langerhans cells in patients with necrolytic migratory erythema
- Follicular mucinosis associated with radiation therapy