Found: 101
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Pseudoainhum and autoamputation associated with lamellar ichthyosis.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Superficial epidermolytic ichthyosis.
- Published in:
- 2015
- By:
- Publication type:
- case study
Effect of tazarotene on ichthyosiform erythroderma of Tay's syndrome.
- Published in:
- 2007
- By:
- Publication type:
- case study
Unilateral nevoid hyperkeratosis of the nipple: a report of two cases.
- Published in:
- 2006
- By:
- Publication type:
- journal article
High Levels of Anxiety, Depression, Risk of Suicide, and Implications for Treatment in Patients with Lamellar Ichthyosis.
- Published in:
- Healthcare (2227-9032), 2023, v. 11, n. 14, p. 2071, doi. 10.3390/healthcare11142071
- By:
- Publication type:
- Article
Netherton Syndrome: A Case Report With Literature Review.
- Published in:
- Journal of Pediatrics Review, 2019, v. 7, n. 4, p. 223, doi. 10.32598/jpr.7.4.223
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- Publication type:
- Article
A Rare Case Report of a Collodion Baby with Severe Hypernatremia.
- Published in:
- 2017
- By:
- Publication type:
- Case Study
Ichthyosis fetalis in a cross-bred lamb.
- Published in:
- Veterinary Dermatology, 2017, v. 28, n. 5, p. 516, doi. 10.1111/vde.12459
- By:
- Publication type:
- Article
Summary of mutations underlying autosomal recessive congenital ichthyoses (ARCI) in Arabs with four novel mutations in ARCI-related genes from the United Arab Emirates.
- Published in:
- International Journal of Dermatology, 2017, v. 56, n. 5, p. 514, doi. 10.1111/ijd.13568
- By:
- Publication type:
- Article
Is it safe to use N-acetylcysteine in the treatment of bilateral ectropion on collodion baby?
- Published in:
- International Journal of Dermatology, 2017, v. 56, n. 4, p. e71, doi. 10.1111/ijd.13456
- By:
- Publication type:
- Article
Novel mutations in TGM1 and ABCA12 cause autosomal recessive congenital ichthyosis in five Saudi families.
- Published in:
- International Journal of Dermatology, 2016, v. 55, n. 6, p. 673, doi. 10.1111/ijd.13279
- By:
- Publication type:
- Article
Genetics Corner: Trichothiodystrophy 1 Causes Neutropenia in an Infant with Congenital ichthyosis and Brittle Hair.
- Published in:
- 2021
- By:
- Publication type:
- Case Study
گزارش يك مورد ايكتيوز دلقكي با يك نتيجه مطلوب: درمان اوليه و بهبودي قابل ملاحظه
- Published in:
- Hayat / Ḥayāt, 2019, v. 24, n. 4, p. 335
- By:
- Publication type:
- Article
Prenatal diagnosis of congenital harlequin ichthyosis with fetal MRI.
- Published in:
- Indian Journal of Radiology & Imaging, 2019, v. 29, n. 4, p. 448, doi. 10.4103/ijri.IJRI_105_19
- By:
- Publication type:
- Article
A 6-Month-Old Boy with Reddish, Scaly Skin: Netherton Syndrome.
- Published in:
- Journal of Pediatric Research, 2018, v. 5, p. 54, doi. 10.4274/jpr.63825
- By:
- Publication type:
- Article
Kollodion bebek olgu serisi: Retinoik asit yüz güldürüyor.
- Published in:
- Türk Pediatri Arşivi, 2018, v. 53, n. 1, p. 51, doi. 10.5152/TurkPediatriArs.2018.3704
- By:
- Publication type:
- Article
Harlequin ichthyosis: The third babies with harlequin ichthyosis in a family.
- Published in:
- 2014
- By:
- Publication type:
- Case Study
Plastic baby with rubber doll-like skin.
- Published in:
- Indian Journal of Health & Wellbeing, 2016, v. 7, n. 2, p. 263
- By:
- Publication type:
- Article
Lichen Planus Pigmentosus and Frontal Fibrosing Alopecia Mimicking Discoid Lupus Erythematosus.
- Published in:
- 2019
- By:
- Publication type:
- Case Study
Expanding the Genotypic Spectrum of Bathing Suit Ichthyosis.
- Published in:
- 2017
- By:
- Publication type:
- journal article
Intrafamily and Interfamilial Phenotype Variation and Immature Immunity in Patients With Netherton Syndrome and Finnish SPINK5 Founder Mutation.
- Published in:
- 2016
- By:
- Publication type:
- journal article
Neonatal Endocrinologic Problems in Collodion Babies.
- Published in:
- Pediatric Dermatology, 2017, v. 34, n. 3, p. 290, doi. 10.1111/pde.13120
- By:
- Publication type:
- Article
Invasive Melanoma in a Patient with Congenital Ichthyosiform Erythroderma.
- Published in:
- Pediatric Dermatology, 2017, v. 34, n. 1, p. e35, doi. 10.1111/pde.13012
- By:
- Publication type:
- Article
Two Cases of Autosomal Recessive Congenital Ichthyosis due to CYP4F22 Mutations: Expanding the Genotype of Self-Healing Collodion Baby.
- Published in:
- Pediatric Dermatology, 2016, v. 33, n. 2, p. e48, doi. 10.1111/pde.12740
- By:
- Publication type:
- Article
Congenital Ichthyosiform Erythroderma Superimposed with Chronic Dermatophytosis: A Report of Three Siblings.
- Published in:
- Pediatric Dermatology, 2016, v. 33, n. 1, p. e6, doi. 10.1111/pde.12728
- By:
- Publication type:
- Article
CHILD Syndrome: Case Report of a Chinese Patient and Literature Review of the NAD[P]H Steroid Dehydrogenase-Like Protein Gene Mutation.
- Published in:
- Pediatric Dermatology, 2015, v. 32, n. 6, p. e277, doi. 10.1111/pde.12701
- By:
- Publication type:
- Article
Ichthyoses: Case series.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Case of the month: a 10-year-old boy with Down syndrome and ichthyosiform changes.
- Published in:
- 1997
- By:
- Publication type:
- journal article
Identification of a novel lethal form of autosomal recessive ichthyosis caused by UDP‐glucose ceramide glucosyltransferase deficiency.
- Published in:
- 2018
- By:
- Publication type:
- Letter to the Editor
What is your diagnosis?
- Published in:
- Journal of the Turkish-German Gynecological Association, 2018, v. 19, n. 1, p. 53, doi. 10.4274/jtgga.2017.0117
- By:
- Publication type:
- Article
Juvenile idiopathic arthritis in infants with Harlequin Ichthyosis: two cases report and literature review.
- Published in:
- Italian Journal of Pediatrics, 2020, v. 46, n. 1, p. 1, doi. 10.1186/s13052-020-0817-5
- By:
- Publication type:
- Article
Opposed-phase MR imaging of lipid storage myopathy in a case of Chanarin-Dorfman disease.
- Published in:
- 2008
- By:
- Publication type:
- journal article
Ashy Dermatosis and Lichen Planus Pigmentosus: The Histopathological Differences.
- Published in:
- BioMed Research International, 2019, p. 1, doi. 10.1155/2019/5829185
- By:
- Publication type:
- Article
Image Gallery: Rapidly spontaneous onset of erythroderma in a neonate.
- Published in:
- 2018
- By:
- Publication type:
- Case Study
Whole-exome sequencing identified a novel frameshift mutation in SDR9C7 underlying autosomal recessive congenital ichthyosis in a Pakistani family.
- Published in:
- British Journal of Dermatology, 2017, v. 177, n. 5, p. e191, doi. 10.1111/bjd.15535
- By:
- Publication type:
- Article
Expanding mutation landscape and phenotypic spectrum of autosomal recessive congenital ichthyosis.
- Published in:
- British Journal of Dermatology, 2017, v. 177, n. 2, p. 342, doi. 10.1111/bjd.15689
- By:
- Publication type:
- Article
Ichthyoses: new insights unravel defects in skin barrier function resulting in diverse clinical and morphological phenotypes.
- Published in:
- British Journal of Dermatology, 2017, v. 176, n. 4, p. 863, doi. 10.1111/bjd.15211
- By:
- Publication type:
- Article
Morphological alterations in two siblings with autosomal recessive congenital ichthyosis associated with CYP4F22 mutations.
- Published in:
- British Journal of Dermatology, 2017, v. 176, n. 4, p. 1068, doi. 10.1111/bjd.14860
- By:
- Publication type:
- Article
Epidermolytic Hyperkeratosis: A Challenging Pathology for Clinical Correlation.
- Published in:
- Balkan Medical Journal, 2019, v. 36, n. 5, p. 294, doi. 10.4274/balkanmedj.galenos.2019.2019.1.127
- By:
- Publication type:
- Article
A Case with Netherton Syndrome-Classical Findings in Late Diagnosis.
- Published in:
- Asthma Allergy Immunology / Astim Allerji Immunoloji, 2022, v. 20, n. 1, p. 64, doi. 10.21911/aai.635
- By:
- Publication type:
- Article
Epidermolytic hyperkeratosis: clinical update.
- Published in:
- Clinical, Cosmetic & Investigational Dermatology, 2019, v. 12, p. 333, doi. 10.2147/CCID.S166849
- By:
- Publication type:
- Article
Congenital Ichthyosis in 14 Great Dane Puppies With a New Presentation.
- Published in:
- Veterinary Pathology, 2016, v. 53, n. 3, p. 614, doi. 10.1177/0300985815595516
- By:
- Publication type:
- Article
Bilateral viral keratitis in lamellar ichthyosis: A rare ocular manifestation.
- Published in:
- 2022
- By:
- Publication type:
- journal article
Combined medical and surgical management for cicatricial ectropion in lamellar ichthyosis: A report of three cases.
- Published in:
- 2020
- By:
- Publication type:
- case study
NIPAL4/ichthyin is expressed in the granular layer of human epidermis and mutated in two Pakistani families with autosomal recessive ichthyosis.
- Published in:
- 2010
- By:
- Publication type:
- journal article
Compound heterozygous ABCA12 mutations including a novel nonsense mutation underlie harlequin ichthyosis.
- Published in:
- 2007
- By:
- Publication type:
- journal article
Regression and disappearance of clinical symptoms in some cases of genodermatoses.
- Published in:
- 1993
- By:
- Publication type:
- journal article
Neonatal Harlequin color change associated with Prostaglandin E<sub>1</sub> administration.
- Published in:
- Pediatrics International, 2021, v. 63, n. 5, p. 610, doi. 10.1111/ped.14581
- By:
- Publication type:
- Article
Airborne transmission from a neonate with Netherton syndrome during an outbreak of MRSA.
- Published in:
- Pediatrics International, 2016, v. 58, n. 6, p. 518, doi. 10.1111/ped.12841
- By:
- Publication type:
- Article
High frequency of primary hereditary ichthyoses in the North-East region of Cairo, Egypt.
- Published in:
- Advances in Dermatology & Allergology / Postępy Dermatologii i Alergologii, 2018, v. 35, n. 2, p. 161, doi. 10.5114/ada.2018.75238
- By:
- Publication type:
- Article