S. Chao

发表

Scleritis and anterior uveitis may herald the development of an epibulbar tumor in patients with extranodal Rosai-Dorfman disease: a case report

Yu-Kuei Lee, S. Chao, Chaw-Ning Lee, 2019, BMC Ophthalmology.

Naevus anaemicus‐like hypopigmented macules in dyskeratosis congenita

S. Chao, Yi‐Pei Lee, Julia Yu‐Yun Lee, 2011, The Australasian journal of dermatology.

A novel splicing mutation of the CYLD gene in a Taiwanese family with multiple familial trichoepithelioma

J. Y. Lee, S. Chao, Tsung-Mao Huang, 2007, Clinical and experimental dermatology.

A retrospective study of pulmonary infarction in patients with systemic lupus erythematosus from southern Taiwan

C. R. Wang, B. Lin, H. Tsai, 2011, Lupus.

Sarcoidosis in Taiwan: clinical characteristics and atypical mycobacteria.

Jin-Jou Yan, S. Chao, Julia Yu‐Yun Lee, 2002, Journal of the Formosan Medical Association = Taiwan yi zhi.

Pneumocystis jirovecii Pneumonia in Systemic Lupus Erythematosus From Southern Taiwan

C. Ou, Wei-Chieh Lin, Jiu-Yao Wang, 2013, Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases.

Novel exon nucleotide substitution at the splice junction causes a neonatal Marfan syndrome

S. Chao, Y.-J. Lin, J-S Chen, 2010, Clinical genetics.

Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation

S. Chao, Julia Yu‐Yun Lee, H. Lin, 2010 .

Mutation report: complete paternal uniparental isodisomy of chromosome 1: a novel mechanism for Herlitz junctional epidermolysis bullosa.

H. Shimizu, J. Uitto, L. Pulkkinen, 2000, The Journal of investigative dermatology.

A Novel Deletion Mutation in the NF1 Gene in a Taiwanese Patient with Neurofibromatosis Type 1

S. Chao, Mei-Hui Yang, Yi-Chen Liao, 2006 .

Cutaneous Manifestations of Human Immunodeficiency Virus Infection in Taiwan

T. Tzung, Chia-Yi Yang, J. Y. Lee, 2004, The Kaohsiung journal of medical sciences.

Early-life or lifetime sun exposure, sun reaction, and the risk of squamous cell carcinoma in an Asian population

Thomas J. Smith, Y. Hsueh, D. Christiani, 2010, Cancer Causes & Control.

Mal de Meleda in a taiwanese.

S. Chao, Julia Yu‐Yun Lee, Mei-Hui Yang, 2005, Journal of the Formosan Medical Association = Taiwan yi zhi.

Collodion baby and loricrin keratoderma: a case report and mutation analysis

M. Yang, S. Chao, J. M. Yeh, 2013, Clinical and experimental dermatology.

PTPN11 mutations in LEOPARD syndrome: report of four cases in Taiwan.

Shio‐Jean Lin, Jieh-Neng Wang, Jing-Ming Wu, 2009, Journal of the Formosan Medical Association = Taiwan yi zhi.

A novel mutation in the keratin 4 gene causing white sponge naevus

J. Y. Lee, S. Chao, M-H Yang, 2003, The British journal of dermatology.

Pachyonychia congenita: Report of two cases and mutation analysis

S. Chao, J. M. Yeh, Ching-Yuang Huang, 2012 .

A novel keratin 9 gene mutation (Asn160His) in a Taiwanese family with epidermolytic palmoplantar keratoderma

J-H Lin, S. Chao, M-H Yang, 2004, Clinical and experimental dermatology.

A novel deletion mutation of the DSRAD gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria

J. Y. Lee, S. Chao, M-H Yang, 2005, The British journal of dermatology.

Novel Mutations in the Helix Termination Motif of Keratin 3 and Keratin 12 in 2 Taiwanese Families with Meesmann Corneal Dystrophy

Ying-Ting Chen, S. Tseng, S. Chao, 2005, Cornea.

Köbner A Novel Mutation in the L 12 Domain of Keratin 5 in the Köbner Variant of Epidermolysis Bullosa Simplex

S. Hsu, S. Chao, Julia Yu‐Yun Lee, 2008 .

A Novel Mutation in the L12 Domain of Keratin 5 in the Kobner Variant of Epidermolysis Bullosa Simplex

S. Hsu, S. Chao, Julia Yu‐Yun Lee, 2005 .

Novel KRT14 mutation in a Taiwanese patient with epidermolysis bullosa simplex (Köbner type).

Shu-fen Lee, S. Chao, Mei-Hui Yang, 2002, Journal of the Formosan Medical Association = Taiwan yi zhi.

BOY WITH EPIDERMOLYSIS BULLOSA SIMPLEX DOWLING-MEARA

J. Uitto, C. Shieh, S. Chao, 2001 .

Hypophosphatemic Rickets Associated with Epidermal Nevus Syndrome and Giant Hairy Nevus

Shio‐Jean Lin, Yen-Yin Chou, Wen-Hui Tsai, 2005, Journal of pediatric endocrinology & metabolism : JPEM.

Congenital Self-Healing Reticulohistiocytosis Mimicking Diffuse Neonatal Hemangiomatosis

S. Chao, Julia Yu‐Yun Lee, Ching-Yuang Huang, 2004, Dermatology.

Netherton syndrome: report of two Taiwanese siblings with staphylococcal scalded skin syndrome and mutation of SPINK5

G. Richard, J. Y. Lee, S. Chao, 2005, The British journal of dermatology.

Hailey‐Hailey disease: a novel mutation of the ATP2C1 gene in a Taiwanese family with divergent clinical presentation

S. Chao, C-C. Wang, T-H Tsai, 2008, Journal of the European Academy of Dermatology and Venereology : JEADV.

Premenstrual exacerbation in calcium ATPase disorders of the skin

O. Szász, R. Szigeti, R. Kellermayer, 2007, Journal of the European Academy of Dermatology and Venereology : JEADV.

Hailey-Hailey Disease Masquerading as Condyloma Acuminatum-Case Report and Novel Mutation Analysis

J. Y. Lee, S. Chao, Yi-Chen Liao, 2005 .

Mutation analysis of ATP2C1 gene in Taiwanese patients with Hailey-Hailey disease.

S. Chao, M-H Yang, Y. Tsai, 2010, The British journal of dermatology.

Mutation analysis of ATP2C1 gene in Taiwanese patients with Hailey–Hailey disease

S. Chao, Mei-Hui Yang, Y. Tsai, 2002 .

Matrix adhesion characteristics of fibroblasts in keloid and hypertrophic scar

T. Wong, S. Chao, Julia Yu‐Yun Lee, 2006 .

Focal dermal hypoplasia: report of a Taiwanese case

S. Chao, Julia Yu‐Yun Lee, Meng-Chi Wu, 2011 .

Widespread cutaneous necrosis associated with antiphospholipid syndrome

I. Jou, Ming-Fei Liu, S. Chao, 1996, Clinical Rheumatology.

High Prevalence of Anal Human Papillomavirus Infection and Associated Risky Behaviors in Men Infected with Human Immunodeficiency Virus in Taiwan

W. Ko, N. Ko, N. Lee, 2013, AIDS and Behavior.

Nodules on the trunk and the arm of an 8-year-old boy

S. Chao, H. Lin, Yi An Chen, 2011 .

Meralgia Paresthetica -Report of Cases and Review of the Literature-

J. Y. Lee, S. Chao, Y. Tsai, 2003 .

Multicentric Reticulohistiocytosis without Arthritis Successfully Treated with Systemic Corticosteroids - A Case Report and Literature Review -

S. Hsu, S. Chao, Julia Yu‐Yun Lee, 2006 .

Use of Tissue Meshing Technique to Facilitate Side to Side Closure of Large Defects

H. Sheu, S. Chao, T. Wong, 1998, Dermatologic surgery : official publication for American Society for Dermatologic Surgery [et al.].

Atypical fibroxanthoma-like amelanotic malignant melanoma: A case report and literature review

S. Shieh, S. Chao, Julia Yu‐Yun Lee, 2013 .

Atypical fi broxanthoma-like amelanotic malignant melanoma : A case report and literature review

S. Shieh, S. Chao, Julia Yu‐Yun Lee, 2013 .

Arsenic Methylation and Skin Cancer Risk in Southwestern Taiwan

Thomas J. Smith, Y. Hsueh, D. Christiani, 2003, Journal of occupational and environmental medicine.

Giant café-au-lait macule in neurofibromatosis 1: a type 2 segmental manifestation of neurofibromatosis 1?

R. Happle, WenChieh Chen, Chao-Chun Yang, 2008, Journal of the American Academy of Dermatology.

Acute cutaneous graft-versus-host disease with ichthyosiform features.

C. Tsao, S. Chao, C. Liu, 1998, The British journal of dermatology.

Cutaneous alternariosis in a renal transplant recipient: a case report and literature review.

Chia-Chi Hsu, S. Chao, Shen-Shin Chang, 2015, Asian journal of surgery.

Evanescent and persistent pruritic eruptions of adult-onset still disease: a clinical and pathologic study of 36 patients.

Ming-Fei Liu, S. Chao, Julia Yu‐Yun Lee, 2012, Seminars in arthritis and rheumatism.

Cutaneous protothecosis: report of five cases

M. Hsu, J. Y. Lee, S. Chao, 2002, The British journal of dermatology.

Human skin surface lipid film: an ultrastructural study and interaction with corneocytes and intercellular lipid lamellae of the stratum corneum

J. Tsai, H. Sheu, S. Chao, 1999, The British journal of dermatology.

Bowen's disease with features resembling myrmecia wart

K. Hsu, S. Chao, Julia Yu‐Yun Lee, 2015, The Journal of dermatology.

Transient zinc deficiency syndrome in a breast-fed infant due to decreased zinc in breast milk (type II hypozincemia of infancy): A case report and review of the literature

S. Chao, Julia Yu‐Yun Lee, Wei-Li Yang, 2012 .

Laminin 5 mutations in junctional epidermolysis bullosa: molecular basis of Herlitz vs non-Herlitz phenotypes

J. Uitto, L. Pulkkinen, D. Murrell, 2001, Human Genetics.

Omenn syndrome: A case report and review of literature

Chia-Chi Hsu, S. Chao, Julia Yu‐Yun Lee, 2011 .

Semi-dominant GPNMB mutations in amyloidosis cutis dyschromica.

M. Simpson, J. Tolar, J. McGrath, 2019, The Journal of investigative dermatology.

Leukemia Cutis in Acute Lymphocytic Leukemia Masquerading as Viral Exanthem

C. Tsao, S. Chao, J. Lee, 1999, The Journal of dermatology.

M. Tsai, Ching-Chi Lee, C. Chi, 2010, Academic emergency medicine : official journal of the Society for Academic Emergency Medicine.

Trichophyton tonsurans infection in Tainan area.

S. Chao, M. Hsu, 1994, Journal of the Formosan Medical Association = Taiwan yi zhi.

Congenital occipital dermal sinus with intracranial dermoid cyst complicated by recurrent Escherichia coli meningitis

Chao-Ching Huang, S. Chao, Meng‐Ying Hsieh, 1998 .

Brittle nails and dyspareunia as first clues to recurrences of malignant glucagonoma

J. Y. Lee, S. Chao, J.Y.‐Y. Lee, 2002, The British journal of dermatology.

A de novo glycine substitution mutation in the collagenous domain of COL7A1 in dominant dystrophic epidermolysis bullosa

J. Uitto, L. Pulkkinen, J. Y. Lee, 2000, Archives of Dermatological Research.

Histopathological Differential Diagnosis of Keloid and Hypertrophic Scar

Chao-Chun Yang, S. Chao, Julia Yu‐Yun Lee, 2004, The American Journal of dermatopathology.

Erythema induratum: a clinicopathologic and polymerase chain reaction study.

J. Y. Lee, S. Chao, J. Yan, 2001, Journal of the Formosan Medical Association = Taiwan yi zhi.

Black lunula caused by Tegafur.

WenChieh Chen, S. Chao, Guan-yu Chen, 2004, Acta dermato-venereologica.

Mutation analysis of the ATP2A2 gene in Taiwanese patients with Darier's disease

S. Chao, J.Y.‐Y. Lee, M‐H. Yang, 2002, The British journal of dermatology.

Transient zinc de fi ciency syndrome in a breast-fed infant due to decreased zinc in breast milk ( type II hypozincemia of infancy ) : A case report and review of the literature

S. Chao, Julia Yu‐Yun Lee, Wei-Li Yang, 2022 .

A novel splice mutation in the ATP2C1 gene in a woman with concomitant psoriasis vulgaris and disseminated Hailey–Hailey disease

M. Hsu, S. Chao, Julia Yu‐Yun Lee, 2012, International journal of dermatology.

Hypersensitivity Syndrome and Pure Red Cell Aplasia Following Allopurinol Therapy in a Patient with Chronic Kidney Disease

Chao-Chun Yang, S. Chao, Julia Yu‐Yun Lee, 2005, The Annals of pharmacotherapy.

WOX1 Is Essential for UVB Irradiation–Induced Apoptosis and Down-Regulated via Translational Blockade in UVB-Induced Cutaneous Squamous Cell Carcinoma In vivo

L. Hsu, N. Chang, Ching-Li Cheng, 2005, Clinical Cancer Research.

Herpes zoster‐associated severity and duration of pain, health‐related quality of life, and healthcare utilization in Taiwan: a prospective observational study

J. Sampalis, K. Kawai, C. Acosta, 2015, International journal of dermatology.

Eosinophilic Cellulitis and Panniculitis with Generalized Vesicular Pustular Id Reaction after a Molten Aluminum Burn

S. Chao, Julia Yu‐Yun Lee, Yi-Pei Lee, 2010, Dermatitis : contact, atopic, occupational, drug.

DKC1 gene mutation in a Taiwanese kindred with X-linked dyskeratosis congenita.

C. Tsao, J. Y. Lee, S. Chao, 2002, The Kaohsiung journal of medical sciences.

Novel compound heterozygous indel ZMPSTE24 mutations in a Taiwanese male infant with restrictive dermopathy

Yi-Han Chang, Meng-Che Tsai, P. Tsai, 2022, The Journal of dermatology.

Anhidrotic ectodermal dysplasia-A case series in a medical center in southern Taiwan

S. Chao, Ching-Yuang Huang, Kuei‐Chung Liu, 2012 .

A novel 7‐bp deletion mutation in a Taiwanese family with X‐linked hypohidrotic ectodermal dysplasia

S. Chao, Tsu-Kung Lin, M-H Lin, 2004, Clinical and experimental dermatology.

Real-world efficacy of biological agents in moderate-to-severe plaque psoriasis: An analysis of 75 patients in Taiwan

E. Lai, Yu-Chen Chen, Yi-Ting Huang, 2020, PloS one.

Mutational analysis of epidermolysis bullosa in Taiwan by whole-exome sequencing complemented by RNA sequencing: a series of 77 patients

J. McGrath, Peng-Chieh Chen, M. Tang, 2022, Orphanet Journal of Rare Diseases.

Kikuchi's Disease (Histiocytic Necrotizing Lymphadenitis) Associated with Cutaneous Lupus Erythematosus

S. Chao, Julia Yu‐Yun Lee, Y. Liao, 2005 .

Follicular mucinosis occurring after bone marrow transplantation in a patient with acute lymphoblastic leukemia.

J. Y. Lee, S. Chao, Y. Tsai, 2004, Journal of the Formosan Medical Association = Taiwan yi zhi.

Erythema multiforme-like secondary syphilis in a HIV-positive bisexual man.

W. Ko, J. Y. Lee, S. Chao, 2010, Acta dermato-venereologica.

Mutations in TRPS1 gene in trichorhinophalangeal syndrome type I in Asian patients

S. Chao, C. Ning, L-H Chen, 2010, The British journal of dermatology.

Clinical characteristics of tricho-rhino-phalangeal syndrome type I in Taiwanese.

J. Y. Lee, S. Chao, C. Ning, 2001, Journal of the Formosan Medical Association = Taiwan yi zhi.

Acute rhabdomyolysis and intravascular hemolysis following extensive wasp stings

S. Chao, Yu-Yun Lee, 1999, International journal of dermatology.

Early Intervention with High-Dose Steroid Pulse Therapy Prolongs Disease-Free Interval of Severe Alopecia Areata: A Retrospective Study

Chun-Te Lee, WenChieh Chen, Chao-Chun Yang, 2013, Annals of dermatology.

Dyschromatosis symmetrica hereditaria: A retrospective case series and literature review

S. Chao, Amy Chia Ying Peng, Yi An Chen, 2013 .

A novel nonsense mutation of the DSRAD gene in a Taiwanese family with dyschromatosis symmetrica hereditaria.

S. Chao, Mei-Hui Yang, Ching-Yuang Huang, 2006, European journal of dermatology : EJD.

A novel mutation of the RNA-specific adenosine deaminase 1 gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria and Becker's nevus-like lesion

Chao-Chun Yang, S. Chao, Mei-Hui Yang, 2016 .

A novel deletion mutation in the adenosine deaminase RNA-specific gene in a Taiwanese patient with dyschromatosis symmetrica hereditaria

S. Chao, Julia Yu‐Yun Lee, Yi An Chen, 2011 .

A 38.8 kb deletion mutation of the iduronate-2-sulfatase gene in a patient with Hunter syndrome.

Shio‐Jean Lin, P. Kuo, Yen-Yin Chou, 2005, Journal of the Formosan Medical Association = Taiwan yi zhi.

Plectin Missense Mutation p.Leu319Pro in the Pathogenesis of Autosomal Recessive Epidermolysis Bullosa Simplex

J. McGrath, Peng-Chieh Chen, K. Natsuga, 2020, Acta dermato-venereologica.

Cutaneous sarcoidosis among Taiwanese.

J. Y. Lee, S. Chao, J. Yan, 2000, Journal of the Formosan Medical Association = Taiwan yi zhi.

A large fungating verruciform xanthoma of the scrotum in association with arteriovenous malformation mimicking giant condyloma

S. Chao, Julia Yu‐Yun Lee, C. Hsu, 2014 .

Keratitis-ichthyosis-deafness syndrome with GJB2 mutation manifesting generalized erythematous plaques of porokeratotic eccrine ostial and dermal duct nevus

Yu-Chen Chen, S. Chao, Julia Yu‐Yun Lee, 2019, Dermatologica Sinica.

Sweet's syndrome in a severely neutropenic patient during therapy with recombinant human granulocyte colony-stimulating factor.

C. Tsao, J. Y. Lee, S. Chao, 1997, Journal of the Formosan Medical Association = Taiwan yi zhi.

Complete Paternal Uniparental Isodisomy of Chromosome 1: A Novel Mechanism for Herlitz Junctional Epidermolysis Bullosa

H. Shimizu, J. Uitto, L. Pulkkinen, 2000 .

Six primary cancers in one lynch syndrome patient with chronic arsenic exposure

B. Lin, S. Chao, Jenq‐Chang Lee, 2012, Journal of surgical oncology.

De novo mutation of keratin 9 gene in two Taiwanese patients with epidermolytic palmoplantar keratoderma.

S. Chao, Julia Yu‐Yun Lee, Mei-Hui Yang, 2003, Journal of the Formosan Medical Association = Taiwan yi zhi.

Identification of OCRL1 mutations in two Taiwanese Lowe syndrome patients.

Y. Chiou, Shio‐Jean Lin, Yen-Yin Chou, 2005, Acta paediatrica Taiwanica = Taiwan er ke yi xue hui za zhi.

Mutation analyses of COL7A1 gene in three Taiwanese patients with severe recessive dystrophic epidermolysis bullosa.

S. Chao, Julia Yu‐Yun Lee, 2007, Journal of the Formosan Medical Association = Taiwan yi zhi.

Capillary morphogenesis gene‐2 mutation in infantile systemic hyalinosis: ultrastructural study and mutation analysis in a Taiwanese infant

J Y-Y Lee, Y-M Tsai, S-C Chao, 2005, Clinical and experimental dermatology.

Acquired dermal melanocytosis of the ear

S. Chao, Julia Yu‐Yun Lee, Chi-Hsuan Chen, 2022, International journal of dermatology.

Weber–Cockayne type of epidermolysis bullosa simplex associated with a novel mutation in keratin 5 and amyloid deposits

W‐R. Lee, S. Chao, Y. Chiang, 2008, The British journal of dermatology.

Telangiectatic metastatic breast carcinoma preceded by en cuirasse metastatic breast carcinoma

C. Tsao, S. Chao, J.Y.‐Y. Lee, 2004, The British journal of dermatology.

Treatment of classical type Kaposi's sarcoma with paclitaxel.

C. Tsao, J. Y. Lee, S. Chao, 2001, Anticancer Research.

Novel exon nucleotide substitution at the splice junction causes a neonatal Marfan syndrome

S. Chao, Y.-J. Lin, Chun-hui Tsai, 2010, Clinical genetics.

Cerebrotendinous xanthomatosis-a case report with novel compound heterozygous mutation of CYP27A1 gene

P. Sung, S. Chao, Julia Yu‐Yun Lee, 2018, Dermatologica Sinica.

Erythroderma with Scaling Patches

S. Chao, Ming-Hsien Lin, Julia Yu‐Yun Lee, 2005 .