| scholarly article | Q13442814 |
| P50 | author | Kohsuke Imai | Q41117654 |
| Anders Fasth | Q45866509 | ||
| Uwe Wintergerst | Q55302608 | ||
| Tomohiro Morio | Q56635449 | ||
| Jeroen G Noordzij | Q59218637 | ||
| Adrian Thrasher | Q60318865 | ||
| Siobhan O Burns | Q60651613 | ||
| Alfons Meindl | Q63015490 | ||
| Shigeaki Nonoyama | Q116781969 | ||
| Bernd H Belohradsky | Q116781980 | ||
| Tanja C Bittner | Q116781983 | ||
| Isabelle Pellier | Q124216720 | ||
| Alain Fischer | Q2636403 | ||
| Hans D. Ochs | Q115437 | ||
| P2093 | author name string | Michael H Albert | |
| Benjamin Gathmann | |||
| Cristina Fillat | |||
| Gabriele Strauss | |||
| Lucia Dora Notarangelo | |||
| Manfred Hoenig | |||
| Michaela Nathrath | |||
| Philipp Pagel | |||
| Teresa Espanol | |||
| P433 | issue | 16 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | thrombocytopenia | Q585285 |
| P304 | page(s) | 3231-3238 | |
| P577 | publication date | 2010-02-19 | |
| P1433 | published in | Blood | Q885070 |
| P1476 | title | X-linked thrombocytopenia (XLT) due to WAS mutations: clinical characteristics, long-term outcome, and treatment options | |
| P478 | volume | 115 |
| Q53407993 | A Novel WASP Gene Mutation in a Chinese Boy with Wiskott-Aldrich Syndrome. |
| Q64108172 | A Systematic Review on Predisposition to Lymphoid (B and T cell) Neoplasias in Patients With Primary Immunodeficiencies and Immune Dysregulatory Disorders (Inborn Errors of Immunity) |
| Q33408705 | A case of familial X-linked thrombocytopenia with a novel WAS gene mutation |
| Q33404827 | A novel Wiskott-Aldrich syndrome protein mutation in an infant with thrombotic thrombocytopenic purpura |
| Q33394391 | A peptide derived from the Wiskott-Aldrich syndrome (WAS) protein-interacting protein (WIP) restores WAS protein level and actin cytoskeleton reorganization in lymphocytes from patients with WAS mutations that disrupt WIP binding |
| Q33433504 | A rare case of Wiskott-Aldrich Syndrome with normal platelet size: a case report |
| Q33439801 | A risk factor analysis of outcomes after unrelated cord blood transplantation for children with Wiskott-Aldrich syndrome |
| Q53205248 | A single-center study of hematopoietic stem cell transplantation for primary immune deficiencies (PIDD). |
| Q42558048 | Adult-onset immunodeficiency--why is it important in rheumatology? |
| Q33411395 | Allogeneic bone marrow transplantation appears to ameliorate IgA nephropathy in a patient with X-linked thrombocytopenia |
| Q33424425 | Analyses of Genetic and Clinical Parameters for Screening Patients With Inherited Thrombocytopenia with Small or Normal-Sized Platelets |
| Q38841123 | Autoimmunity and Primary Immunodeficiency Disorders. |
| Q36101320 | Autoimmunity in wiskott-Aldrich syndrome: an unsolved enigma |
| Q33426239 | Broad spectrum of autoantibodies in patients with Wiskott-Aldrich syndrome and X-linked thrombocytopenia |
| Q60907816 | CRISPR/Cas9-mediated deletion of the Wiskott-Aldrich syndrome locus causes actin cytoskeleton disorganization in murine erythroleukemia cells |
| Q55043161 | Chronic nephritis associated with X-linked thrombocytopenia. |
| Q45873782 | Clinical Manifestations and Pathophysiological Mechanisms of the Wiskott-Aldrich Syndrome. |
| Q33403644 | Clinical and molecular characterization of Thai patients with Wiskott-Aldrich syndrome. |
| Q33392815 | Clinical spectrum, pathophysiology and treatment of the Wiskott–Aldrich syndrome |
| Q33424297 | Current and emerging treatment options for Wiskott-Aldrich syndrome |
| Q33422383 | Diagnosis and treatment of inherited thrombocytopenias. |
| Q89804990 | Diagnosis of Inherited Platelet Disorders on a Blood Smear |
| Q30545781 | Disease-associated missense mutations in the EVH1 domain disrupt intrinsic WASp function causing dysregulated actin dynamics and impaired dendritic cell migration |
| Q33417841 | Disruption of hSWI/SNF complexes in T cells by WAS mutations distinguishes X-linked thrombocytopenia from Wiskott-Aldrich syndrome |
| Q33424820 | Effects of eltrombopag on platelet count and platelet activation in Wiskott-Aldrich syndrome/X-linked thrombocytopenia |
| Q91621150 | Eltrombopag for the treatment of inherited thrombocytopenias: a phase II clinical trial |
| Q34778685 | Exome sequencing identifies a novel FOXP3 mutation in a 2-generation family with inflammatory bowel disease |
| Q33402780 | Genetics of familial forms of thrombocytopenia |
| Q33418658 | Hematopoietic Stem Cell Transplantation for X-Linked Thrombocytopenia With Mutations in the WAS gene |
| Q92802115 | Hematopoietic Stem Cell Transplantation in Primary Immunodeficiency Diseases: Current Status and Future Perspectives |
| Q47210347 | Hematopoietic cell transplantation in primary immunodeficiency - conventional and emerging indications |
| Q44797357 | Hematopoietic stem cell transplantation for primary immunodeficiency diseases |
| Q49989075 | Hereditary thrombocytopenias: a growing list of disorders |
| Q38195246 | ICON: the early diagnosis of congenital immunodeficiencies |
| Q34755351 | IL-2 induces a WAVE2-dependent pathway for actin reorganization that enables WASp-independent human NK cell function. |
| Q33397878 | IVS6+5G>A found in Wiskott-Aldrich syndrome and X-linked thrombocytopenia in a Korean family |
| Q33396427 | Inherited platelet disorders: a clinical approach to diagnosis and management |
| Q33432109 | Inherited thrombocytopenias-recent advances in clinical and molecular aspects |
| Q33410845 | Intermittent X-linked thrombocytopenia with a novel WAS gene mutation |
| Q33442914 | Intermittent low platelet counts hampering diagnosis of X-linked thrombocytopenia in children: report of two unrelated cases and a novel mutation in the gene coding for the Wiskott-Aldrich syndrome protein |
| Q64039650 | Lentiviral gene therapy corrects platelet phenotype and function in Wiskott-Aldrich patients |
| Q33395718 | Long-term outcome and lineage-specific chimerism in 194 patients with Wiskott-Aldrich syndrome treated by hematopoietic cell transplantation in the period 1980-2009: an international collaborative study |
| Q33422658 | Molecular basis of inherited thrombocytopenias |
| Q33395963 | Monozygotic twin pair showing discordant phenotype for X-linked thrombocytopenia and Wiskott-Aldrich syndrome: a role for epigenetics? |
| Q33391541 | Novel clearance mechanisms of platelets |
| Q34063501 | Nuclear role of WASp in gene transcription is uncoupled from its ARP2/3-dependent cytoplasmic role in actin polymerization. |
| Q33407443 | Pathogenesis and management of inherited thrombocytopenias: rationale for the use of thrombopoietin-receptor agonists |
| Q33402440 | Platelets from WAS patients show an increased susceptibility to ex vivo phagocytosis |
| Q90252292 | Primary immunodeficiencies and their associated risk of malignancies in children: an overview |
| Q38557638 | Prolonged survival after splenectomy in Wiskott-Aldrich syndrome: a case report |
| Q49722119 | R-loops cause genomic instability in T helper lymphocytes from patients with Wiskott-Aldrich syndrome |
| Q53086157 | Rare autoimmune disorders with Mendelian inheritance. |
| Q34832611 | Relevance of laboratory testing for the diagnosis of primary immunodeficiencies: a review of case-based examples of selected immunodeficiencies |
| Q36115749 | SUMOylation-disrupting WAS mutation converts WASp from a transcriptional activator to a repressor of NF-κB response genes in T cells |
| Q33421912 | Successful renal transplantation in a patient with a Wiskott-Aldrich syndrome protein (WASP) gene mutation |
| Q43969022 | The European internet-based patient and research database for primary immunodeficiencies: update 2011. |
| Q36225715 | The genomic landscape of juvenile myelomonocytic leukemia |
| Q37767175 | The relationship of x-linked primary immune deficiencies and autoimmunity |
| Q33405198 | Two cases of Wiskott-Aldrich syndrome in neonates due to gene mutations |
| Q35995198 | Ubiquitous high-level gene expression in hematopoietic lineages provides effective lentiviral gene therapy of murine Wiskott-Aldrich syndrome |
| Q26852216 | WIP remodeling actin behind the scenes: how WIP reshapes immune and other functions |
| Q92239402 | When WAS Gene Diagnosis Is Needed: Seeking Clues Through Comparison Between Patients With Wiskott-Aldrich Syndrome and Idiopathic Thrombocytopenic Purpura |
| Q92406277 | Whole Exome Sequencing of an X-linked Thrombocytopenia Patient with Normal Sized Platelets |
| Q36632359 | Wiskott-Aldrich Syndrome at the nexus of autoimmune and primary immunodeficiency diseases |
| Q90657085 | Wiskott-Aldrich syndrome protein senses irradiation-induced DNA damage to coordinate the cell-protective Golgi dispersal response in human T and B lymphocytes |
| Q38151844 | Wiskott-Aldrich syndrome protein--dynamic regulation of actin homeostasis: from activation through function and signal termination in T lymphocytes |
| Q33422471 | Wiskott-Aldrich syndrome/X-linked thrombocytopenia in China: Clinical characteristic and genotype-phenotype correlation |
| Q33406620 | Wiskott-Aldrich syndrome: a comprehensive review |
| Q33415221 | Wiskott-Aldrich syndrome: diagnosis, current management, and emerging treatments |
| Q33417294 | X-linked thrombocytopenia in three males with normal sized platelets due to novel WAS gene mutations |
| Q54694891 | [Wiskott-Aldrich syndrome with special phenotypes: report of 3 cases]. |
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