Related references
Note: Only part of the references are listed.Incontinentia pigmenti in adults
Angela E. Scheuerle
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2019)
Cardiopulmonary anomalies in incontinentia pigmenti patients
Giuliana Onnis et al.
INTERNATIONAL JOURNAL OF DERMATOLOGY (2018)
Postzygotic mosaicism and incontinentia pigmenti in male patients: molecular diagnosis yield
Z. Alabdullatif et al.
BRITISH JOURNAL OF DERMATOLOGY (2018)
Intrafamilial clinical variability in four families with incontinentia pigmenti
Luiza M. Mariath et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2018)
A case of reversible pulmonary arterial hypertension associated with incontinentia pigmenti
Veronique Atallah et al.
PULMONARY CIRCULATION (2018)
Dental anomalies in 14 patients with IP: clinical and radiological analysis and review
Fernanda D. Santa-Maria et al.
CLINICAL ORAL INVESTIGATIONS (2017)
Incontinentia pigmenti. Herpes simplex infection as an important differential diagnosis in the neonatal period
A. -C. Rosenthal et al.
HAUTARZT (2017)
Copy Number Variants in Patients with Autism and Additional Clinical Features: Report of VIPR2 Duplication and a Novel Microduplication Syndrome
Saghar Ghasemi Firouzabadi et al.
MOLECULAR NEUROBIOLOGY (2017)
Cognitive-behavioural phenotype in a group of girls from 1.2 to 12 years old with the Incontinentia Pigmenti syndrome: Recommendations for clinical management
Maria Rosa Pizzamiglio et al.
APPLIED NEUROPSYCHOLOGY-CHILD (2017)
Lack of interaction between NEMO and SHARPIN impairs linear ubiquitination and NF-κB activation and leads to incontinentia pigmenti
Elodie Bal et al.
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY (2017)
Incontinentia Pigmenti: A Summary Review of This Rare Ectodermal Dysplasia With Neurologic Manifestations, Including Treatment Protocols
Carol Greene-Roethke
JOURNAL OF PEDIATRIC HEALTH CARE (2017)
Severe neuroimaging anomalies are usually associated with random X inactivation in leucocytes circulating DNA in X-linked dominant Incontinentia Pigmenti
Volodia Dangouloff-Ros et al.
MOLECULAR GENETICS AND METABOLISM (2017)
Unusual Father-to-Daughter Transmission of Incontinentia Pigmenti Due to Mosaicism in IP Males
Francesca Fusco et al.
PEDIATRICS (2017)
Unique subungueal keratoacanthoma revealing incontinentia pigmenti
M. Ferneiny et al.
JOURNAL OF THE EUROPEAN ACADEMY OF DERMATOLOGY AND VENEREOLOGY (2016)
A brain microvasculature endothelial cell-specific viral vector with the potential to treat neurovascular and neurological diseases
Jakob Koerbelin et al.
EMBO MOLECULAR MEDICINE (2016)
Effectiveness of Corticosteroid Therapy for Acute Neurological Symptoms in Incontinentia Pigmenti
Seiichi Tomotaki et al.
PEDIATRIC NEUROLOGY (2016)
Somatic Mosaicism of a Novel IKBKG Mutation in a Male Patient with Incontinentia Pigmenti
Sarah Hull et al.
AMERICAN JOURNAL OF MEDICAL GENETICS PART A (2015)
High-Dose Glucocorticoid Therapy in the Management of Seizures in Neonatal Incontinentia Pigmenti: A Case Report
David S. Wolf et al.
JOURNAL OF CHILD NEUROLOGY (2015)
Incontinentia pigmenti
Claudia Schermann Poziomczyk et al.
ANAIS BRASILEIROS DE DERMATOLOGIA (2014)
Incontinentia pigmenti diagnostic criteria update
S. Minic et al.
CLINICAL GENETICS (2014)
Insight into IKBKG/NEMO Locus: Report of New Mutations and Complex Genomic Rearrangements Leading to Incontinentia Pigmenti Disease
Matilde Immacolata Conte et al.
HUMAN MUTATION (2014)
Incontinentia Pigmenti in an XY Boy: Case Report and Review of the Literature
Erin Mullan et al.
JOURNAL OF CUTANEOUS MEDICINE AND SURGERY (2014)
Incontinentia pigmenti: report on data from 2000 to 2013
Francesca Fusco et al.
ORPHANET JOURNAL OF RARE DISEASES (2014)
Incontinentia Pigmenti: Learning Disabilities Are a Fundamental Hallmark of the Disease
Maria Rosa Pizzamiglio et al.
PLOS ONE (2014)
Common Variants on Xq28 Conferring Risk of Schizophrenia in Han Chinese
Emily H. M. Wong et al.
SCHIZOPHRENIA BULLETIN (2014)
Dental and oral anomalies in incontinentia pigmenti: a systematic review
Snezana Minic et al.
CLINICAL ORAL INVESTIGATIONS (2013)
Clinical Utility Gene Card for: incontinentia pigmenti
Francesca Fusco et al.
EUROPEAN JOURNAL OF HUMAN GENETICS (2013)
Systematic review of central nervous system anomalies in incontinentia pigmenti
Snezana Minic et al.
ORPHANET JOURNAL OF RARE DISEASES (2013)
Neurological findings in incontinentia pigmenti; a review
Marije E. C. Meuwissen et al.
EUROPEAN JOURNAL OF MEDICAL GENETICS (2012)
Genomic architecture at the Incontinentia Pigmenti locus favours de novo pathological alleles through different mechanisms
Francesca Fusco et al.
HUMAN MOLECULAR GENETICS (2012)
Incontinentia pigmenti-ophthalmological observation of a series of cases and review of the literature
M. O'Doherty et al.
BRITISH JOURNAL OF OPHTHALMOLOGY (2011)
Clinical and histologic features of incontinentia pigmenti in adults with nuclear factor-κB essential modulator gene mutations
Smail Hadj-Rabia et al.
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY (2011)
Early indirect laser photocoagulation to induce regression of retinal vascular abnormalities in incontinentia pigmenti
Figen Batioglu et al.
ACTA OPHTHALMOLOGICA (2010)
Regression of Retinal Neovascularization After Laser Photocoagulation in Incontinentia Pigmenti
Tushar M. Ranchod et al.
RETINA-THE JOURNAL OF RETINAL AND VITREOUS DISEASES (2010)
Ocular Anomalies in Incontinentia Pigmenti: Literature Review and Meta-Analysis
Snezana Minic et al.
SRPSKI ARHIV ZA CELOKUPNO LEKARSTVO (2010)
Therapeutic use of topical corticosteroids in the vesiculobullous lesions of incontinentia pigmenti
T. I. Kaya et al.
CLINICAL AND EXPERIMENTAL DERMATOLOGY (2009)
Skin biopsy is helpful for the diagnosis of incontinentia pigmenti at late stage (IV): a series of 26 cutaneous biopsies
Sylvie Fraitag et al.
JOURNAL OF CUTANEOUS PATHOLOGY (2009)
Retinal sequelae of incontinentia pigmenti
Chandrakumar Balaratnasingam et al.
PEDIATRICS INTERNATIONAL (2009)
Detection of HPV-15 in painful subungual tumors of incontinentia pigmenti: successful topical therapy with retinoic acid
Pietro Donati et al.
EUROPEAN JOURNAL OF DERMATOLOGY (2009)
Alterations of the IKBKG locus and diseases: An update and a report of 13 novel mutations
Francesca Fusco et al.
HUMAN MUTATION (2008)
Fluorescein angiographic findings in a male infant with incontinentia pigmenti
Giselle DeVetten et al.
JOURNAL OF AAPOS (2007)
Molecular genetics of bipolar disorder and depression
Tadafumi Kato
PSYCHIATRY AND CLINICAL NEUROSCIENCES (2007)
Clinical diagnosis of incontinentia pigmenti in a cohort of male patients
Francesca Fusco et al.
JOURNAL OF THE AMERICAN ACADEMY OF DERMATOLOGY (2007)
Single cell co-amplification of polymorphic markers for the indirect preimplantation genetic diagnosis of hemophilia A, X-linked adrenoleukodystrophy, X-linked hydrocephalus and incontinentia pigmenti loci on Xq28
N Gigarel et al.
HUMAN GENETICS (2004)
Molecular analysis of the genetic defect in a large cohort of IP patients and identification of novel NEMO mutations interfering with NF-κB activation
F Fusco et al.
HUMAN MOLECULAR GENETICS (2004)
A novel PCR approach for prenatal detection of the common NEMO rearrangement in incontinentia pigmenti
J Steffann et al.
PRENATAL DIAGNOSIS (2004)
Clinical study of 40 cases of incontinentia pigmenti
S Hadj-Rabia et al.
ARCHIVES OF DERMATOLOGY (2003)
Late recurrence of inflammatory first-stage lesions in incontinentia pigmenti - An unusual phenomenon and a fascinating pathologic mechanism
N Bodak et al.
ARCHIVES OF DERMATOLOGY (2003)
Two cases of misinterpretation of molecular results in incontinentia pligmenti, and a PCR-based method to discriminate NEMO/IKK gamma gene deletion
T Bardaro et al.
HUMAN MUTATION (2003)
Laser photocoagulation in preproliferative retinopathy of incontinentia pigmenti
JK Nguyen et al.
JOURNAL OF AAPOS (2001)