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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1973 1
1974 2
1975 2
1976 3
1977 2
1979 2
1981 2
1983 2
1984 1
1985 1
1987 1
1988 1
1998 1
1999 2
2002 1
2005 1
2009 1
2010 1
2011 2
2012 1
2013 1
2015 4
2017 1
2018 2
2019 1
2020 2
2021 2
2022 2
2024 0

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43 results

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Page 1
Inflammatory linear verrucous epidermal nevus (ILVEN) encompasses a spectrum of inflammatory mosaic disorders.
Atzmony L, Ugwu N, Hamilton C, Paller AS, Zech L, Antaya RJ, Choate KA. Atzmony L, et al. Pediatr Dermatol. 2022 Nov;39(6):903-907. doi: 10.1111/pde.15094. Epub 2022 Jul 19. Pediatr Dermatol. 2022. PMID: 35853659 Free PMC article.
OBJECTIVE: To elucidate the genetic cause of a cohort of patients diagnosed based on clinical and histopathological evaluation with ILVEN. METHODS: We recruited patients diagnosed with ILVEN based on clinical and histopathological criteria. ...Two patients were re-d …
OBJECTIVE: To elucidate the genetic cause of a cohort of patients diagnosed based on clinical and histopathological evaluation with I …
Vulnerable child syndrome in the neonatal intensive care unit: A review and a new preventative intervention with feasibility and parental satisfaction data.
Hoge MK, Heyne E, Nicholson TF, Acosta D, Mir I, Brown LS, Shaw RJ, Chalak L, Heyne R. Hoge MK, et al. Early Hum Dev. 2021 Mar;154:105283. doi: 10.1016/j.earlhumdev.2020.105283. Epub 2020 Nov 25. Early Hum Dev. 2021. PMID: 33514479 Review.
Vulnerable Child Syndrome (VCS) occurs in the setting in which a child recovers from a life-threatening illness, as result of which the parent develops heightened parental perceptions of child vulnerability (PPCV). ...Parents of premature infants have been shown to …
Vulnerable Child Syndrome (VCS) occurs in the setting in which a child recovers from a life-threatening illness, as result of …
Pathogenesis-based therapies in ichthyoses.
Lai-Cheong JE, Elias PM, Paller AS. Lai-Cheong JE, et al. Dermatol Ther. 2013 Jan-Feb;26(1):46-54. doi: 10.1111/j.1529-8019.2012.01528.x. Dermatol Ther. 2013. PMID: 23384020 Free PMC article. Review.
The translation of these laboratory findings into effective therapies for affected individuals has been slow, however, in large part due to the risk of carcinogenesis from random viral genomic integration and the lack of efficacy of topically applied genetic material and m …
The translation of these laboratory findings into effective therapies for affected individuals has been slow, however, in large part due to …
Childhood interstitial lung disease: A systematic review.
Hime NJ, Zurynski Y, Fitzgerald D, Selvadurai H, Phu A, Deverell M, Elliott EJ, Jaffe A. Hime NJ, et al. Pediatr Pulmonol. 2015 Dec;50(12):1383-92. doi: 10.1002/ppul.23183. Epub 2015 Apr 30. Pediatr Pulmonol. 2015. PMID: 25931270 Review.
Red child syndrome.
Salazar de Sousa J, Almeida V, Bray Pinheiro J. Salazar de Sousa J, et al. Arch Dis Child. 1987 Nov;62(11):1181. doi: 10.1136/adc.62.11.1181. Arch Dis Child. 1987. PMID: 2961311 Free PMC article.
The hyperactive child syndrome.
Weiss G, Hechtman L. Weiss G, et al. Science. 1979 Sep 28;205(4413):1348-54. doi: 10.1126/science.472752. Science. 1979. PMID: 472752
CHILD syndrome: A modified pathogenesis-targeted therapeutic approach.
Bergqvist C, Abdallah B, Hasbani DJ, Abbas O, Kibbi AG, Hamie L, Kurban M, Rubeiz N. Bergqvist C, et al. Am J Med Genet A. 2018 Mar;176(3):733-738. doi: 10.1002/ajmg.a.38619. Epub 2018 Feb 2. Am J Med Genet A. 2018. PMID: 29392821
Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects (CHILD syndrome) is a rare X-linked dominant genodermatosis caused by mutations in the NAD(P) dependent steroid dehydrogenase-like protein gene. Its defect leads to accumulation of toxic metabolic in …
Congenital Hemidysplasia with Ichthyosiform nevus and Limb Defects (CHILD syndrome) is a rare X-linked dominant genodermatosis …
Rapid improvement of skin lesions in CHILD syndrome with topical 5% simvastatin ointment.
Kallis P, Bisbee E, Garganta C, Schoch JJ. Kallis P, et al. Pediatr Dermatol. 2022 Jan;39(1):151-152. doi: 10.1111/pde.14865. Epub 2021 Nov 17. Pediatr Dermatol. 2022. PMID: 34787337
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome is a rare X-linked dominant disorder of cholesterol synthesis characterized by unilateral ichthyosiform dermatitis with ipsilateral limb hypoplasia. ...
Congenital hemidysplasia with ichthyosiform erythroderma and limb defects (CHILD) syndrome is a rare X-linked dominant disorde …
The hyperactive child syndrome.
Reece RM. Reece RM. Am Fam Physician. 1973 Sep;8(3):98-103. Am Fam Physician. 1973. PMID: 4729718 No abstract available.
43 results