Literature DB >> 16551788

Growth hormone deficiency in Sturge-Weber syndrome.

R S Miller1, K L Ball, A M Comi, E L Germain-Lee.   

Abstract

Sturge-Weber syndrome (SWS) is a disorder involving central nervous system abnormalities that may increase the risk of hypothalamic-pituitary dysfunction. Records of 19 patients with suspected growth hormone deficiency (GHD), identified from a registry of 1653 patients with SWS, were reviewed; nine patients with GHD were found.

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Year:  2006        PMID： 16551788      PMCID： PMC2065976          DOI： 10.1136/adc.2005.082578

Source DB:  PubMed          Journal:  Arch Dis Child        ISSN： 0003-9888            Impact factor:   3.791


  4 in total

1.  An unusual case of Sturge-Weber syndrome.

Authors:  V R Billson; G L Gillam
Journal:  Pathology       Date:  1984-10       Impact factor: 5.306

2.  Vascular malformation of hypothalamus: a cause of isolated growth hormone deficiency.

Authors:  J D Russell; P H Wise; H G Rischbieth
Journal:  Pediatrics       Date:  1980-08       Impact factor: 7.124

3.  Utah Growth Study: growth standards and the prevalence of growth hormone deficiency.

Authors:  R Lindsay; M Feldkamp; D Harris; J Robertson; M Rallison
Journal:  J Pediatr       Date:  1994-07       Impact factor: 4.406

4.  Sturge-Weber syndrome. A case with thyroid and choroid plexus hemangiomas and leptomeningeal melanosis.

Authors:  M S Bentz; J Towfighi; S Greenwood; R Zaino
Journal:  Arch Pathol Lab Med       Date:  1982-02       Impact factor: 5.534
  4 in total
  10 in total

1.  Cell proliferation and oxidative stress pathways are modified in fibroblasts from Sturge-Weber syndrome patients.

Authors:  Shilpa D Kadam; Marjan Gucek; Robert N Cole; Paul A Watkins; Anne M Comi
Journal:  Arch Dermatol Res       Date:  2012-03-10       Impact factor: 3.017

Review 2.  Current Therapeutic Options in Sturge-Weber Syndrome.

Authors:  Anne Comi
Journal:  Semin Pediatr Neurol       Date:  2015-11-11       Impact factor: 1.636

Review 3.  Presentation, diagnosis, pathophysiology, and treatment of the neurological features of Sturge-Weber syndrome.

Authors:  Anne M Comi
Journal:  Neurologist       Date:  2011-07       Impact factor: 1.398

4.  Focal venous hypertension as a pathophysiologic mechanism for tissue hypertrophy, port-wine stains, the Sturge-Weber syndrome, and related disorders: proof of concept with novel hypothesis for underlying etiological cause (an American Ophthalmological Society thesis).

Authors:  Cameron F Parsa
Journal:  Trans Am Ophthalmol Soc       Date:  2013-09

5.  Sturge-weber syndrome.

Authors:  Catherine D Bachur; Anne M Comi
Journal:  Curr Treat Options Neurol       Date:  2013-10       Impact factor: 3.598

Review 6.  Updates and future horizons on the understanding, diagnosis, and treatment of Sturge-Weber syndrome brain involvement.

Authors:  Warren Lo; Douglas A Marchuk; Karen L Ball; Csaba Juhász; Lori C Jordan; Joshua B Ewen; Anne Comi
Journal:  Dev Med Child Neurol       Date:  2011-12-23       Impact factor: 5.449

Review 7.  Sturge-Weber syndrome: an update on the relevant issues for neurosurgeons.

Authors:  Federico Bianchi; Anna Maria Auricchio; Domenica Immacolata Battaglia; Daniela Rosaria Pia Chieffo; Luca Massimi
Journal:  Childs Nerv Syst       Date:  2020-06-21       Impact factor: 1.475

Review 8.  Epilepsy Mechanisms in Neurocutaneous Disorders: Tuberous Sclerosis Complex, Neurofibromatosis Type 1, and Sturge-Weber Syndrome.

Authors:  Carl E Stafstrom; Verena Staedtke; Anne M Comi
Journal:  Front Neurol       Date:  2017-03-17       Impact factor: 4.003

9.  Sturge-Weber syndrome coexisting with polydactyly: a case report.

Authors:  Hongxi Wang; Nana Dong; Li Tan; Chukai Huang
Journal:  BMC Ophthalmol       Date:  2021-01-06       Impact factor: 2.209

Review 10.  Less known aspects of central hypothyroidism: Part 2 - Congenital etiologies.

Authors:  Salvatore Benvenga; Marianne Klose; Roberto Vita; Ulla Feldt-Rasmussen
Journal:  J Clin Transl Endocrinol       Date:  2018-09-27
  10 in total

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