Cargando…

Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports: Erratum

Detalles Bibliográficos
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Wolters Kluwer Health 2016
Materias:	Erratum
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4839872/ https://www.ncbi.nlm.nih.gov/pubmed/31265561 http://dx.doi.org/10.1097/01.md.0000482689.36580.ef

Ejemplares similares

Total Hemi-overgrowth in Pigmentary Mosaicism of the (Hypomelanosis of) Ito Type: Eight Case Reports
por: Pavone, Vito, et al.
Publicado: (2016)

Hypomelanosis of Ito with a trisomy 2 mosaicism: a case report
por: Ponti, Giovanni, et al.
Publicado: (2014)

HYPOMELANOSIS OF ITO: A CASE REPORT
por: Gupta, Monisha, et al.
Publicado: (2002)

A case of hypomelanosis of Ito accompanied by unilateral abnormal limb overgrowth and delayed speech
por: Ozcetin, Mustafa, et al.
Publicado: (2018)

Hypomelanosis of Ito with Multiple Congenital Anomalies
por: Yu, Da-Ae, et al.
Publicado: (2019)

Retinoblastoma Presenting in a Child with Hypomelanosis of Ito
por: El-Sawy, Tarek, et al.
Publicado: (2011)

Hypomelanosis of Ito with an unusual pulmonary abnormality in an infant
por: Bhat, Ramesh Y., et al.
Publicado: (2014)

Hypomelanosis of Ito presenting with pediatric orthopedic issues: a case report
por: Trägårdh, Malene, et al.
Publicado: (2014)

Possible Correlation between Hypomelanosis of Ito and Wilms' Tumor
por: Bello-Germino, Daniella, et al.
Publicado: (2018)

An Interesting Coexistence of Multifocal Hypertrichosis and Hirsutism in Hypomelanosis of Ito
por: Mendiratta, Vibhu, et al.
Publicado: (2019)

Clinical spectrum of MTOR-related hypomelanosis of Ito with neurodevelopmental abnormalities
por: Carmignac, Virginie, et al.
Publicado: (2021)

PIGMENTARY MOSAICISM: AN UPDATE
por: Thapa, Rajoo
Publicado: (2008)

Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito
por: Cunha, Karina S., et al.
Publicado: (2016)

A Rare Concomitance of Two Blaschkoid Pigmentary Disorders: A Juggle of Pigmentary Mosaicism
por: Daroach, Manju, et al.
Publicado: (2019)

Acral speckled hypomelanosis
por: Aldhalaan, Jumana, et al.
Publicado: (2019)

Erratum to: Eight-Year Experience with Minimally Invasive Cardiothoracic Surgery
por: Iribarne, Alexander, et al.
Publicado: (2009)

Erratum: High current density GaAs/Si rectifying heterojunction by defect free Epitaxial Lateral overgrowth on Tunnel Oxide from nano-seed
por: Renard, Charles, et al.
Publicado: (2016)

Erratum to: Familial chromosomal translocation X; 22 associated with infertility and recurrent X mosaicism
por: Grzesiuk, Juliana Dourado, et al.
Publicado: (2016)

The outcome of human mosaic aneuploid blastocysts after intrauterine transfer A retrospective study: Erratum
Publicado: (2022)

Erratum: Capturing the wide variety of impaired fracture healing phenotypes in Neurofibromatosis Type 1 with eight key factors: a computational study
por: Carlier, A., et al.
Publicado: (2017)

Successful treatment of progressive macular hypomelanosis
por: Leonard, Nicholas, et al.
Publicado: (2020)

Transient cutaneous hypomelanosis after cryoanesthesia
por: Pippi, Roberto, et al.
Publicado: (2022)

Pigmentary mosaicism: a review of original literature and recommendations for future handling
por: Kromann, Anna Boye, et al.
Publicado: (2018)

Disappearing pigmentary mosaicism during imatinib treatment for gastrointestinal stromal tumors
por: Coleman, Emily, et al.
Publicado: (2019)

Erratum: Posterior shoulder instability following anatomic total shoulder arthroplasty: A case report and review of management
Publicado: (2016)

Erratum to “Spinocerebellar ataxia type 40: A case report and literature review”
por: Han, Fengyue, et al.
Publicado: (2022)

Erratum: The History of Biomechanics in Total Hip Arthroplasty
Publicado: (2017)

Pigmentary mosaicism as a recurrent clinical manifestation in three new patients with mosaic trisomy 12 diagnosed postnatally: cases report and literature review
por: Martínez-Hernández, A., et al.
Publicado: (2022)

Erratum: CRISPR-engineered mosaicism rapidly reveals that loss of Kcnj13 function in mice mimics human disease phenotypes
por: Zhong, Hua, et al.
Publicado: (2015)

Propionibacterium Acnes Phylogenetic Type III is Associated with Progressive Macular Hypomelanosis
por: Petersen, Rolf L. W., et al.
Publicado: (2017)

Erratum to: Ataxia with Oculomotor Apraxia Type 1 without Oculomotor Apraxia: A Case Report
por: Lee, Minwoo, et al.
Publicado: (2017)

Smile rejuvenation: A case report: Erratum
por: Gopikrishna, Velayutham
Publicado: (2014)

Perianal atypical leiomyoma: A case report: Erratum
Publicado: (2018)

Umbilical artery thrombosis: Two case reports: Erratum
Publicado: (2020)

Erratum to: Cardiac arrest, chronic total occlusion and occluded stent in a 16-year-old boy with Kawasaki disease: a case report
Publicado: (2020)

Erratum to: Imaging the implant-soft tissue interactions in total knee arthroplasty
por: Bonnin, Michel P., et al.
Publicado: (2016)

Erratum: Patient Expectations of Sexual Activity After Total Hip Arthroplasty
Publicado: (2018)

Erratum to “Sensor-Assisted Total Knee Arthroplasty: A Narrative Review”
por: Park, Cheol Hee, et al.
Publicado: (2021)

Therapeutic wounding - 88% phenol in idiopathic guttate hypomelanosis
por: Ravikiran, Shilpashree P., et al.
Publicado: (2014)

Surgical Outcome of Spinal Neurilemmoma: Two Case Reports: Erratum
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_gffqnck467ar8t638b29uo70r3