about
Syndromic (phenotypic) diarrhea in early infancyElastase 2 is expressed in human and mouse epidermis and impairs skin barrier function in Netherton syndrome through filaggrin and lipid misprocessingLocalization of the Netherton syndrome gene to chromosome 5q32, by linkage analysis and homozygosity mapping.KLK5 Inactivation Reverses Cutaneous Hallmarks of Netherton SyndromeHair shaft videodermoscopy in netherton syndromeNetherton syndrome: report of two Taiwanese siblings with staphylococcal scalded skin syndrome and mutation of SPINK5Hair on a gene string: recent advances in understanding the molecular genetics of hair loss.Netherton syndrome - Why ENT surgeons should be aware of this rare disease - report of a case.Immunoglobulin E in primary immunodeficiency diseases.Comèl-Netherton syndrome defined as primary immunodeficiency.Ichthyosis linearis circumflexa and Netherton's syndrome with idiopathic dwarfismPrenatal diagnosis of Comel-Netherton syndrome with PGD, case report and review article.Inherited ichthyosiform dermatoses in childhood.Netherton's syndrome.Inherited ichthyoses/generalized Mendelian disorders of cornification.Kallikrein 5 induces atopic dermatitis-like lesions through PAR2-mediated thymic stromal lymphopoietin expression in Netherton syndrome.Transgenic kallikrein 5 mice reproduce major cutaneous and systemic hallmarks of Netherton syndrome.A practical, algorithmic approach to diagnosing hair shaft disorders.Malignant skin tumours in patients with inherited ichthyosis.The atopic march: current insights into skin barrier dysfunction and epithelial cell-derived cytokines.Central osteosclerosis with ectodermal dysplasia: clinical, laboratory, radiologic, and histopathologic characterization with review of the literature.Inherited ichthyosis: Syndromic forms.Genetics of eosinophilic esophagitis.Neuroichthyosis with hypogonadism (Rud's syndrome).Human hair: a genetic marker.Phage Therapy in a 16-Year-Old Boy with Netherton Syndrome.Bubble hair.Bamboo Hair in Netherton's Syndrome.Migratory polycyclic lesions with facial eczema since infancy.Squamous cell carcinoma in a patient with Netherton's syndrome.Comèl-Netherton syndrome complicated by papillomatous skin lesions containing human papillomaviruses 51 and 52 and plane warts containing human papillomavirus 16.Association of SPINK5 gene polymorphisms with atopic dermatitis in the Japanese population.Netherton syndrome: mutation analysis of two Taiwanese families.Prenatal diagnosis of a lethal form of Netherton syndrome by SPINK5 mutation analysis.An infant with Netherton syndrome and persistent pulmonary hypertension requiring extracorporeal membrane oxygenation.Netherton syndrome with extensive skin peeling and failure to thrive due to a homozygous frameshift mutation in SPINK5.Netherton syndrome in two Japanese siblings with a novel mutation in the SPINK5 gene: immunohistochemical studies of LEKTI and other epidermal molecules.Infliximab therapy for Netherton syndrome: A case report.Updated strategies for the management, pathogenesis and molecular genetics of different forms of ichthyosis syndromes with prominent hair abnormalities.Intractable diarrhea of infancy with facial dysmorphism, trichorrhexis nodosa, and cirrhosis.
P2860
Q21202896-CA48BF97-78AD-4C04-BD56-7AA9758AAF6EQ24300787-EC08BFEB-DE44-4F10-8BFC-A5D95C156135Q24539101-EFBF885D-79D7-48B7-9179-2892DA56CF41Q27310680-CB959993-6482-4FF6-92A4-9193304ABB35Q28256329-0FAE3AB2-F7E4-4CA2-A9C4-0377520F0528Q28303020-CC210384-C661-4E85-B2AB-3D3CF56447DFQ34190527-726AAB9C-DD8F-4BBD-AFB5-7853A9F1C585Q34800165-4EBCB9FF-8E97-44EC-BCD1-34CB7737735CQ34929232-B5743863-350F-4272-B80E-2C038CF38965Q34997608-1A36B37A-3444-4D5F-B36A-E9A394FD8823Q35143941-9BBC25C6-BE06-4073-8ACD-159D2DACF55DQ35181937-ECA4EAB8-4C64-4081-A86E-DEC25CED0ED5Q35907345-79D9F438-7656-47AE-BC44-C89B21E266C5Q36061813-4EAD15F9-CAB6-4DBF-A1A2-4D30BCD20DE5Q36543023-EC8CE296-2151-4236-AF61-0A2C23C69BE9Q37273142-BCE14263-533C-4310-A684-6F7E628058B2Q37630234-26A72600-4307-4AA0-8AF8-5495C54EFACDQ37823641-06DEB8A6-C533-443E-91F1-46E94AD36E6AQ37868636-4AB3C9D1-230A-431D-B51B-F7AD787C4BF6Q38704374-6611DA42-8063-439A-9FB3-0242A8DFC3B4Q38753948-01F73586-8DFF-400C-84CD-92872154BEC8Q38761870-AE9C9310-5A13-4FE0-8B53-C304BDFE513FQ39146390-867127C7-974F-45D6-BAB0-0361E374284EQ39337391-C944F713-1C25-4844-986C-ED70D711BC9EQ39991929-E84829F5-0562-4B14-9C66-C1261FFD7B43Q40119098-EEA636AA-98CF-4E72-BE6E-1E3ADA60CD69Q42104700-8D83E9EA-16CE-4A01-BB98-FD59F21E5326Q42427342-18A7CE1D-2DE8-4665-9B52-F24E5908704DQ42663243-7F7F32AC-FB73-458B-A2C2-0D8CB7A6934BQ43852409-9140FE4D-AB11-4A9C-8A06-BF692131BC24Q44444121-D1B9A550-8AE6-434F-8093-708BDAF7176CQ44444282-300686D8-8B57-4A22-A521-578E788F768AQ44634320-783F9637-6CA6-43DC-A844-7ED7EDBB2129Q45714543-33CB616B-6D13-4F43-950A-02AF4401C70FQ46040416-56B6BC3F-7F4C-4605-BBEA-9CA43477E058Q46533645-70DFF5E2-7D5B-4BCE-B472-58AF5B622D2FQ46753322-97ECC734-2287-4F10-A8C6-63885DF67B9BQ47118602-94224BA0-F5B4-4A43-A2B4-BD76C153090AQ47693815-6C8363FC-305E-4D39-82DE-3B39F3F02749Q51946487-789DF6E7-385C-4274-8615-ECCFAC84ADBF
P2860
description
1958 nî lūn-bûn
@nan
1958年の論文
@ja
1958年論文
@yue
1958年論文
@zh-hant
1958年論文
@zh-hk
1958年論文
@zh-mo
1958年論文
@zh-tw
1958年论文
@wuu
1958年论文
@zh
1958年论文
@zh-cn
name
A unique case of trichorrhexis nodosa; bamboo hairs.
@en
type
label
A unique case of trichorrhexis nodosa; bamboo hairs.
@en
prefLabel
A unique case of trichorrhexis nodosa; bamboo hairs.
@en
P1476
A unique case of trichorrhexis nodosa; bamboo hairs.
@en
P2093
NETHERTON EW
P304
P356
10.1001/ARCHDERM.1958.01560100059009
P577
1958-10-01T00:00:00Z