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Expression Patterns of Clock Gene mRNAs and Clock Proteins in Human Psoriatic Skin Samples

International journal of molecular sciences, 2021-12, Vol.23 (1), p.121

2021

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Complexity of the Immune Response Elicited by Different COVID-19 Vaccines, in the Light of Natural Autoantibodies and Immunomodulatory Therapies

International journal of molecular sciences, 2023-03, Vol.24 (7), p.6439

2023

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Content validity of the EQ-5D-5L with skin irritation and self-confidence bolt-ons in patients with atopic dermatitis: a qualitative think-aloud study

Quality of life research, 2024, Vol.33 (1), p.101-111

2024

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Homozygous ITGA3 Missense Mutation in Adults in a Family with Syndromic Epidermolysis Bullosa (ILNEB) without Pulmonary Involvement

Journal of investigative dermatology, 2021-11, Vol.141 (11), p.2752-2756

2021

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Pustulosis acuta generalisata with mucosal and joint involvement associated with polyspecific autoantibodies

EJD. European journal of dermatology, 2016-11, Vol.26 (6), p.624-626

2016

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Clinical, Laboratory and Histological Features of Dipeptidyl Peptidase-4 Inhibitor Related Noninflammatory Bullous Pemphigoid

Journal of clinical medicine, 2021-04, Vol.10 (9), p.1916

2021

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Amoxicillin rash in patients with infectious mononucleosis: evidence of true drug sensitization

Allergy, asthma, and clinical immunology, 2015-01, Vol.11 (1), p.1-1, Article 1

2015

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Subjective well-being in patients with pemphigus: a path analysis

The European journal of health economics, 2019-06, Vol.20 (Suppl 1), p.S101-S107

2019

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A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities

Archives of Dermatological Research, 2012-10, Vol.304 (8), p.679-681

2012

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A mutational hotspot in CYLD causing cylindromas: a comparison of phenotypes arising in different genetic backgrounds

Acta dermato-venereologica, 2013-11, Vol.93 (6), p.743-745

2013

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A newly identified missense mutation of the EDA1 gene in a Hungarian patient with Christ–Siemens–Touraine syndrome

Archives of Dermatological Research, 2014, Vol.306 (1), p.97-100

2014

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Ulcus vulvae acutum Lipschütz in two young female patients

EJD. European journal of dermatology, 2014-05, Vol.24 (3), p.361-364

2014

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Bowel-associated dermatosis-arthritis syndrome ― a relapsing, extremely rare extraintestinal sign of acute flare-up in Crohn's disease

EJD. European journal of dermatology, 2011-05, Vol.21 (3), p.443-445

2011

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COP1 Contributes to UVB-Induced Signaling in Human Keratinocytes

Journal of investigative dermatology, 2010-02, Vol.130 (2), p.541-545

2010

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Allopurinol-induced hypersensitivity syndrome

Orvosi hetilap, 2012-04, Vol.153 (15), p.586

2012

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The measurement performance of the EQ-5D-5L versus EQ-5D-3L in patients with hidradenitis suppurativa

Quality of life research, 2021-05, Vol.30 (5), p.1477-1490

2021

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Resource utilization, work productivity and costs in patients with hidradenitis suppurativa: a cost-of-illness study

Expert review of pharmacoeconomics & outcomes research, 2022-04, Vol.22 (3), p.399-408

2022

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A novel missense mutation of the CYLD gene identified in a Hungarian family with Brooke-Spiegler syndrome

Experimental dermatology, 2012-12, Vol.21 (12), p.967-969

2012

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Successful Treatment of Multiple Basaliomas with Bleomycin-based Electrochemotherapy: A Case Series of Three Patients with Gorlin-Goltz Syndrome

Acta dermato-venereologica, 2012-11, Vol.92 (6), p.648-651

2012

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COP1 Contributes to UVB-Induced Signaling in Human Keratinocytes

Kinyó, Ágnes

2011

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ProQuest

Allopurinol is the most common cause of DRESS syndrome in Hungarian patients

Clinical and translational allergy, 2014-07, Vol.4 (S3), p.P17-n/a

2014

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Strontium Ranelate-induced DRESS Syndrome with Persistent Autoimmune Hepatitis

Acta dermato-venereologica, 2011-03, Vol.91 (2), p.205-206

2011

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A novel missense mutation of the CYLD gene identified in a H ungarian family with B rooke– S piegler syndrome

Experimental dermatology, 2012-12, Vol.21 (12), p.967-969

2012

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Amoxicillin rash in patients with infectious mononucleosis: evidence of true drug sensitization

Allergy, asthma, and clinical immunology : official journal of the Canadian Society of Allergy and Clinical Immunology, 2015, Vol.11 (1), p.1-1

2015

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Granuloma Annulare

European Handbook of Dermatological Treatments, p.345-356

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Expression Patterns of Clock Gene mRNAs and Clock Proteins in Human Psoriatic Skin Samples

Complexity of the Immune Response Elicited by Different COVID-19 Vaccines, in the Light of Natural Autoantibodies and Immunomodulatory Therapies

Content validity of the EQ-5D-5L with skin irritation and self-confidence bolt-ons in patients with atopic dermatitis: a qualitative think-aloud study

Homozygous ITGA3 Missense Mutation in Adults in a Family with Syndromic Epidermolysis Bullosa (ILNEB) without Pulmonary Involvement

Pustulosis acuta generalisata with mucosal and joint involvement associated with polyspecific autoantibodies

Clinical, Laboratory and Histological Features of Dipeptidyl Peptidase-4 Inhibitor Related Noninflammatory Bullous Pemphigoid

Amoxicillin rash in patients with infectious mononucleosis: evidence of true drug sensitization

Subjective well-being in patients with pemphigus: a path analysis

A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities

A mutational hotspot in CYLD causing cylindromas: a comparison of phenotypes arising in different genetic backgrounds

A newly identified missense mutation of the EDA1 gene in a Hungarian patient with Christ–Siemens–Touraine syndrome

Ulcus vulvae acutum Lipschütz in two young female patients

Bowel-associated dermatosis-arthritis syndrome ― a relapsing, extremely rare extraintestinal sign of acute flare-up in Crohn's disease

COP1 Contributes to UVB-Induced Signaling in Human Keratinocytes

Allopurinol-induced hypersensitivity syndrome

The measurement performance of the EQ-5D-5L versus EQ-5D-3L in patients with hidradenitis suppurativa

Resource utilization, work productivity and costs in patients with hidradenitis suppurativa: a cost-of-illness study

A novel missense mutation of the CYLD gene identified in a Hungarian family with Brooke-Spiegler syndrome

Successful Treatment of Multiple Basaliomas with Bleomycin-based Electrochemotherapy: A Case Series of Three Patients with Gorlin-Goltz Syndrome

COP1 Contributes to UVB-Induced Signaling in Human Keratinocytes

Allopurinol is the most common cause of DRESS syndrome in Hungarian patients

Strontium Ranelate-induced DRESS Syndrome with Persistent Autoimmune Hepatitis

A novel missense mutation of the CYLD gene identified in a H ungarian family with B rooke– S piegler syndrome

Amoxicillin rash in patients with infectious mononucleosis: evidence of true drug sensitization

Granuloma Annulare

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