Genetic Signature of Acute Lymphoblastic Leukemia and Netherton Syndrome Co-incidence-First Report in the Literature

scientific article published on 01 January 2019

Genetic Signature of Acute Lymphoblastic Leukemia and Netherton Syndrome Co-incidence-First Report in the Literature is …
instance of (P31):
case reportQ2782326
scholarly articleQ13442814

External links are
P356DOI10.3389/FONC.2019.01477
P932PMC publication ID6978700
P698PubMed publication ID32010610

P50authorJerzy Roman KowalczykQ21328387
Michał KorostyńskiQ67880705
Kinga KwiecinskaQ90964014
Marcin PiechotaQ96058271
Walentyna BalwierzQ102361240
Szymon SkoczeńQ125172866
Angelina Moryl-BujakowskaQ125173024
Wojciech MłynarskiQ30903317
P2093author name stringWojciech Strojny
Konrad Stepien
Piotr Centkowski
Elzbieta Wyrobek
Magdalena Rej
P2860cites workHuman papillomavirus infection in Netherton's syndromeQ73895182
Cushing syndrome from percutaneous absorption of 1% hydrocortisone ointment in Netherton syndromeQ79774717
Penile cancer in a man with netherton syndromeQ40163272
Netherton's syndrome: a syndrome of elevated IgE and characteristic skin and hair findingsQ40570245
Netherton syndrome with multiple non-melanoma skin cancersQ42436922
Significant absorption of topical tacrolimus in 3 patients with Netherton syndrome.Q43639646
Impact of TRPV3 on the development of allergic dermatitis as a dendritic cell modulatorQ45381582
JAK2 aberrations in childhood B-cell precursor acute lymphoblastic leukemiaQ47095048
TRPV3 Channel in Keratinocytes in Scars with Post-Burn PruritusQ47096526
Considerations in surgical management of a Buschke-Lowenstein tumor in Netherton syndrome: A case reportQ47343035
The effects of R683S (G) genetic mutations on the JAK2 activity, structure and stability.Q50925561
A preliminary study of new single polymorphisms in the T helper type 17 pathway for psoriasis in the Korean population.Q51367413
Philadelphia Chromosome-like Acute Lymphoblastic Leukemia.Q54989161
Infliximab Infusions for Netherton Syndrome: Sustained Clinical Improvement Correlates with a Reduction of Thymic Stromal Lymphopoietin Levels in the SkinQ61843707
Genetic Profile and Clinical Implications of Hepatoblastoma and Neuroblastoma Coexistence in a ChildQ64076272
Genome instability syndromes caused by impaired DNA repair and aberrant DNA damage responsesQ64389645
Localization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.Q24539101
Ribosomal protein L5 and L11 mutations are associated with cleft palate and abnormal thumbs in Diamond-Blackfan anemia patientsQ24643416
Mutations in SPINK5, encoding a serine protease inhibitor, cause Netherton syndromeQ28145552
Revised nomenclature and classification of inherited ichthyoses: results of the First Ichthyosis Consensus Conference in Sorèze 2009.Q34126886
Outcomes of children with BCR-ABL1–like acute lymphoblastic leukemia treated with risk-directed therapy based on the levels of minimal residual diseaseQ34172033
Targetable kinase-activating lesions in Ph-like acute lymphoblastic leukemiaQ34314927
6MP adherence in a multiracial cohort of children with acute lymphoblastic leukemia: a Children's Oncology Group studyQ34318474
Comèl-Netherton syndrome defined as primary immunodeficiencyQ34997608
A Patient with Congenital Ichthyosis Hystrix (Disseminated Congenital Naevus) and Acute Lymphoblastic LeukaemiaQ35105476
Olmsted syndrome: clinical, molecular and therapeutic aspectsQ35215730
Incidence of neoplasia in Diamond Blackfan anemia: a report from the Diamond Blackfan Anemia Registry.Q35909685
Primary Immunodeficiency Diseases: an Update on the Classification from the International Union of Immunological Societies Expert Committee for Primary Immunodeficiency 2015.Q36319898
Hereditary cancer predisposition in children: genetic basis and clinical implicationsQ36461758
Nonadherence to oral mercaptopurine and risk of relapse in Hispanic and non-Hispanic white children with acute lymphoblastic leukemia: a report from the children's oncology groupQ36695870
B-cell acute lymphoblastic leukemia associated with SET-NUP214 rearrangement: A case report and review of the literatureQ36740935
Genetic predispositions to childhood leukemia.Q37073895
JAK mutations in high-risk childhood acute lymphoblastic leukemiaQ37224111
Malignant skin tumours in patients with inherited ichthyosisQ37868636
Netherton syndrome: skin inflammation and allergy by loss of protease inhibitionQ38076305
TRPV3.Q38206427
NUP214 fusion genes in acute leukemia (Review).Q38239669
Netherton Syndrome: A Genotype-Phenotype ReviewQ39025260
Ph-like acute lymphoblastic leukemiaQ39027852
Risk-adjusted therapy of acute lymphoblastic leukemia can decrease treatment burden and improve survival: treatment results of 2169 unselected pediatric and adolescent patients enrolled in the trial ALL-BFM 95.Q39835436
Intrafamily and Interfamilial Phenotype Variation and Immature Immunity in Patients With Netherton Syndrome and Finnish SPINK5 Founder Mutation.Q40006125
P275copyright licenseCreative Commons Attribution 4.0 InternationalQ20007257
P6216copyright statuscopyrightedQ50423863
P921main subjectNetherton syndromeQ9390284
lymphoblastic leukemiaQ18553852
P304page(s)1477
P577publication date2019-01-01
P1433published inFrontiers in OncologyQ26839986
P1476titleGenetic Signature of Acute Lymphoblastic Leukemia and Netherton Syndrome Co-incidence-First Report in the Literature
P478volume9

Reverse relations

Q96954627Polymorphisms of SLC19A1 80 G>A, MTHFR 677 C>T, and Tandem TS Repeats Influence Pharmacokinetics, Acute Liver Toxicity, and Vomiting in Children With Acute Lymphoblastic Leukemia Treated With High Doses of Methotrexatecites workP2860

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