Reema L Habiby

  • 880 Citations
19952020

Research output per year

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Research Output

2020

Turner Syndrome Systematic Review: Spontaneous Thelarche and Menarche Stratified by Karyotype

Dabrowski, E., Jensen, R., Johnson, E. K., Habiby, R. L., Brickman, W. J. & Finlayson, C., Feb 1 2020, In : Hormone Research in Paediatrics. 92, 3, p. 143-149 7 p.

Research output: Contribution to journalReview article

Turner Syndrome with Y Chromosome: Spontaneous Thelarche, Menarche, and Risk of Malignancy

Dabrowski, E., Johnson, E. K., Patel, V., Hsu, Y. C., Davis, S., Goetsch, A. L., Habiby, R., Brickman, W. J. & Finlayson, C., Feb 2020, In : Journal of pediatric and adolescent gynecology. 33, 1, p. 10-14 5 p.

Research output: Contribution to journalArticle

1 Scopus citations
2018

Pediatric Central Nervous System Tumor Diagnosis, Complications, and Emergencies

Lenzen, A., Garcia Sosa, R. M., Habiby, R., DiPatri, A. J. & Smiley, N. P., Jun 2018, In : Clinical Pediatric Emergency Medicine. 19, 2, p. 153-161 9 p.

Research output: Contribution to journalArticle

2016

Extensive miRNA expression analysis in craniopharyngiomas

Samis, J., Vanin, E. F., Sredni, S. T., de Bonaldo, M. D. F., Costa, F. F., Tomita, T., Habiby, R., Zimmerman, D. & Soares, M. B., Sep 1 2016, In : Child's Nervous System. 32, 9, p. 1617-1624 8 p.

Research output: Contribution to journalArticle

5 Scopus citations
5 Scopus citations
2011
23 Scopus citations
2008

Leydig Cell Adenoma

Finlayson, C., Habiby, R. & Zimmerman, D., 2008, A Case-Based Guide to Clinical Endocrinology. Davies, TF. (ed.). New Jersey: Humana Press, p. 453-458

Research output: Chapter in Book/Report/Conference proceedingChapter

2006

Central and gonadal hypogonadism in X-linked lissencephaly

Halac, I., Habiby, R., Curran, J. & Zimmerman, D., Jul 2006, In : Journal of Pediatric Endocrinology and Metabolism. 19, 7, p. 955-957 3 p.

Research output: Contribution to journalArticle

4 Scopus citations
2005

Disorders of the Endocrine System

Zimmerman, D., Habiby, RL. & Brickman, WH., 2005, Pediatrics: Just the Facts. Green, TP., Franklin, WH. & Tanz, RR. (eds.). New York: McGraw-Hill, p. 263-304

Research output: Chapter in Book/Report/Conference proceedingChapter

2001

A novel mutation (Q40P) in PAX8 associated with congenital hypothyroidism and thyroid hypoplasia: Evidence for phenotypic variability in mother and child

Congdon, T., Nguyen, L. Q., Nogueira, C. R., Habiby, R. L., Medeiros-Neto, G. & Kopp, P. A., Jan 1 2001, In : Journal of Clinical Endocrinology and Metabolism. 86, 8, p. 3962-3967 6 p.

Research output: Contribution to journalArticle

105 Scopus citations

Missense mutations cluster within the carboxyl-terminal region of DAX-1 and impair transcriptional repression

Achermann, J. C., Ito, M., Silverman, B. L., Habiby, R. L., Pang, S., Rosler, A. & Jameson, J. L., Aug 2 2001, In : Journal of Clinical Endocrinology and Metabolism. 86, 7, p. 3171-3175 5 p.

Research output: Contribution to journalArticle

66 Scopus citations
2000

Presymptomatic diagnosis of X-linked adrenal hypoplasia congenita by analysis of DAX1

Achermann, J. C., Silverman, B. L., Habiby, R. L. & Jameson, J. L., Jan 1 2000, In : Journal of Pediatrics. 137, 6, p. 878-881 4 p.

Research output: Contribution to journalArticle

49 Scopus citations
1999

Clinical and functional effects of mutations in the DAX-1 gene in patients with adrenal hypoplasia congenita

Reutens, A. T., Achermann, J. C., Ito, M., Ito, M., Gu, W. X., Habiby, R. L., Donohoue, P. A., Pang, S., Hindmarsh, P. C. & Jameson, J. L., Feb 17 1999, In : Journal of Clinical Endocrinology and Metabolism. 84, 2, p. 504-511 8 p.

Research output: Contribution to journalArticle

128 Scopus citations

Mutational analysis of DAX1 in patients with hypogonadotropic hypogonadism or pubertal delay

Achermann, J. C., Gu, W. X., Kotlar, T. J., Meeks, J. J., Sabacan, L. P., Seminara, S. B., Habiby, R. L., Hindmarsh, P. C., Bick, D. P., Sherins, R. J., Crowley, W. F., Layman, L. C. & Jameson, J. L., Jan 1 1999, In : Journal of Clinical Endocrinology and Metabolism. 84, 12, p. 4497-4500 4 p.

Research output: Contribution to journalArticle

71 Scopus citations
1997

Neurofibromatosis type I and precocious puberty: Beyond the chasm [2] (multiple letters)

Habiby, R., Silverman, B., Listernick, R., Cbarrow, J. & Zacbarin, M., Jan 1 1997, In : Journal of Pediatrics. 131, 5, p. 786-787 2 p.

Research output: Contribution to journalLetter

8 Scopus citations
1996

Adrenal hypoplasia congenita with hypogonadotropic hypogonadism: Evidence that DAX-1 mutations lead to combined hypothalamic and pituitary defects in gonadotropin production

Habiby, R. L., Boepple, P., Nachtigall, L., Sluss, P. M., Crowley, W. F. & Jameson, J. L., Aug 15 1996, In : Journal of Clinical Investigation. 98, 4, p. 1055-1062 8 p.

Research output: Contribution to journalArticle

220 Scopus citations

A single-sample, subcutaneous gonadotropin-releasing hormone test for central precocious puberty

Eckert, K. L., Wilson, D. M., Bachrach, L. K., Anhalt, H., Habiby, R. L., Olney, R. C., Hintz, R. L. & Neely, E. K., Apr 1 1996, In : Pediatrics. 97, 4, p. 517-519 3 p.

Research output: Contribution to journalArticle

46 Scopus citations

Precocious puberty, growth hormone deficiency, and neurofibromatosis [5]

Vassilopoulou-Sellin, R., Habiby, R., Silverman, B., Listernick, R. & Charrow, J., Jan 1 1996, In : Journal of Pediatrics. 128, 1, 1 p.

Research output: Contribution to journalLetter

1995

Bone mineral density during treatment of central precocious puberty

Neely, E. K., Bachrach, L. K., Hintz, R. L., Habiby, R. L., Slemenda, C. W., Feezle, L. & Pescovitz, O. H., Nov 1995, In : The Journal of pediatrics. 127, 5, p. 819-822 4 p.

Research output: Contribution to journalArticle

54 Scopus citations

Precocious puberty in children with neurofibromatosis type 1

Habiby, R., Silverman, B., Listernick, R. & Charrow, J., Jan 1 1995, In : The Journal of pediatrics. 126, 3, p. 364-367 4 p.

Research output: Contribution to journalArticle

95 Scopus citations