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N Jospe

Showing results (1-10 of 20) with videos related to

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Pediatrics in Review|November 1, 1996
Fluids and electrolytes--clinical aspectsN Jospe, G Forbes
Pediatrics|August 1, 1990
Growth hormone deficiency in an 8-year-old girl with human immunodeficiency virus infectionN Jospe, K R Powell
Pediatric Dermatology|June 1, 1994
Melanocytic nevi in Turner syndromeB Becker, N Jospe, L A Goldsmith
Acta Paediatrica (Oslo, Norway : 1992). Supplement|March 1, 1993
Temporal and individual variations in the dose of glucocorticoid used for the treatment of salt-losing congenital virilizing adrenal hyperplasia due to 21-hydroxylase deficiencyR Sandrini, N Jospe, C J Migeon
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 1, 1995
Comparison of transdermal and oral estrogen therapy in girls with Turner's syndromeN Jospe, C C Orlowski, R W Furlanetto
Clinical Endocrinology|August 1, 1996
Homozygous nonsense mutation in the insulin receptor gene of a patient with severe congenital insulin resistance: leprechaunism and the role of the insulin-like growth factor receptorN Jospe, P B Kaplowitz, R W Furlanetto
Mental Retardation|September 3, 1999
Ambiguity of the external genitalia in an infant with Down syndrome: gender assignment and ethical implicationsN Jospe, A Lane, J Greenlaw, et al.
Genomics|October 1, 1989
Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21BP A Donohoue, N Jospe, C J Migeon, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 12, 2001
Hyponatremia secondary to reset osmostat in a child with a central nervous system midline defect and a chromosomal abnormalityP Gupta, G Mick, C T Fong, et al.
Journal of Endocrinological Investigation|February 1, 1988
Factitious transient neonatal hyperthyrotropinemiaN Jospe, G D Berkovitz, L E Corcoran, et al.
Pageof 2

Showing results (1-10 of 20) with videos related to

Sort By:
Pageof 2
Pediatrics in Review|November 1, 1996
Fluids and electrolytes--clinical aspectsN Jospe, G Forbes
Pediatrics|August 1, 1990
Growth hormone deficiency in an 8-year-old girl with human immunodeficiency virus infectionN Jospe, K R Powell
Pediatric Dermatology|June 1, 1994
Melanocytic nevi in Turner syndromeB Becker, N Jospe, L A Goldsmith
Acta Paediatrica (Oslo, Norway : 1992). Supplement|March 1, 1993
Temporal and individual variations in the dose of glucocorticoid used for the treatment of salt-losing congenital virilizing adrenal hyperplasia due to 21-hydroxylase deficiencyR Sandrini, N Jospe, C J Migeon
Journal of Pediatric Endocrinology & Metabolism : JPEM|April 1, 1995
Comparison of transdermal and oral estrogen therapy in girls with Turner's syndromeN Jospe, C C Orlowski, R W Furlanetto
Clinical Endocrinology|August 1, 1996
Homozygous nonsense mutation in the insulin receptor gene of a patient with severe congenital insulin resistance: leprechaunism and the role of the insulin-like growth factor receptorN Jospe, P B Kaplowitz, R W Furlanetto
Mental Retardation|September 3, 1999
Ambiguity of the external genitalia in an infant with Down syndrome: gender assignment and ethical implicationsN Jospe, A Lane, J Greenlaw, et al.
Genomics|October 1, 1989
Two distinct areas of unequal crossingover within the steroid 21-hydroxylase genes produce absence of CYP21BP A Donohoue, N Jospe, C J Migeon, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|January 12, 2001
Hyponatremia secondary to reset osmostat in a child with a central nervous system midline defect and a chromosomal abnormalityP Gupta, G Mick, C T Fong, et al.
Journal of Endocrinological Investigation|February 1, 1988
Factitious transient neonatal hyperthyrotropinemiaN Jospe, G D Berkovitz, L E Corcoran, et al.
Pageof 2