Eileen Lange

Eileen Lange

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Eileen Lange

Eileen Lange

Publications by authors named "Eileen Lange"

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10Publications

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Clinical Evaluation of Melorheostosis in the Context of a Natural History Clinical Study.

JBMR Plus 2019 Aug 26;3(8):e10214. Epub 2019 Jul 26.

Clinical and Investigative Orthopedics Surgery Unit National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), NIH Bethesda MD USA.

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http://dx.doi.org/10.1002/jbm4.10214DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6715778PMC
August 2019

Distinct Clinical and Pathological Features of Melorheostosis Associated With Somatic MAP2K1 Mutations.

J Bone Miner Res 2019 Jan 14;34(1):145-156. Epub 2018 Sep 14.

Clinical and Investigative Orthopedics Surgery Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS), National Institutes of Health (NIH), Bethesda, MD, USA.

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http://doi.wiley.com/10.1002/jbmr.3577
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http://dx.doi.org/10.1002/jbmr.3577DOI Listing
January 2019

Somatic activating mutations in MAP2K1 cause melorheostosis.

Nat Commun 2018 04 11;9(1):1390. Epub 2018 Apr 11.

Clinical and Investigative Orthopedics Surgery Unit, National Institute of Arthritis and Musculoskeletal and Skin Diseases, National Institutes of Health, Bethesda, MD, 20892, USA.

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http://dx.doi.org/10.1038/s41467-018-03720-zDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5895796PMC
April 2018

Isolated Large Cell Calcifying Sertoli Cell Tumor in a Young Boy, not Associated with Peutz-Jeghers Syndrome or Carney Complex.

Ann Clin Lab Res 2015;3(1)

Section on Endocrinology and Genetics, Program on Developmental Endocrinology Genetics (PDEGEN), Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD), USA ; Inter-Institute Pediatric Endocrinology Training Program, National Institutes of Health (NIH), Bethesda, MD 20892, USA.

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http://www.aclr.com.es/clinical-research/isolated-large-cell
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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4648613PMC
January 2015

Deletion of 8q24 in an adult with mild dysmorphic features, developmental delay, and ketotic hypoglycemia.

Am J Med Genet A 2010 Jun;152A(6):1545-9

Medical Genetics Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1002/ajmg.a.33395DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2914310PMC
June 2010

An unusual presentation of pediatric Cushing disease: recurrent corticotropinoma of the posterior pituitary lobe.

J Pediatr Endocrinol Metab 2010 Jun;23(6):607-12

Section on Endocrinology and Genetics, Program on Developmental Endocrinology Genetics (PDEGEN), Eunice Kennedy Shriver National Institute of Child Health & Human Development (NICHD), National Institutes of Health (NIH), Bethesda, MD 20892, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4727444PMC
http://dx.doi.org/10.1515/jpem.2010.100DOI Listing
June 2010

Sexual function in women with Turner syndrome.

J Womens Health (Larchmt) 2008 Jan-Feb;17(1):27-33

Developmental Endocrinology Branch, National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1089/jwh.2007.0488DOI Listing
June 2008