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F Lorenzen

Showing results (1-10 of 14) with videos related to

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Ceskoslovenska Pediatrie|January 1, 1994
[Long-term therapy of true precocious puberty in girls using Decapetyl-Depot, a superactive gonadoliberin agonist in depot microcapsulated form]W G Sippell, C J Partsch, R Hümmelink, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1989
[The significance and characteristics of the LHRH test in diagnosing precocious puberty development in girls: the stimulated LH/FSH quotient differentiates between central precocious puberty and premature thelarche]C J Partsch, R Hümmelink, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1979
"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasiaM I New, F Lorenzen, S Pang, et al.
Lancet (London, England)|June 2, 1990
Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examinationM Peter, W G Sippell, F Lorenzen, et al.
Military Medicine|May 1, 1993
A prototype multidisciplinary cancer screening clinic for the military medical facilityD W Johnson, J J Twidwell, R Henderson, et al.
Pediatric Research|December 1, 1979
Hormonal phenotype and HLA-genotype in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency)F Lorenzen, S Pang, M I New, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1980
Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasiaS Pang, L S Levine, F Lorenzen, et al.
Prenatal Diagnosis|February 1, 1988
HLA-A,B,C,DR typing and 17-OHP determination for second trimester prenatal diagnosis of 21-hydroxylase deficient CAHH Grosse-Wilde, E Valentine-Thon, U Vögeler, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1982
Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasiaB Kohn, L S Levine, M S Pollack, et al.
American Journal of Human Genetics|July 1, 1981
HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiencyM S Pollack, L S Levine, G J O'Neill, et al.
Pageof 2

Showing results (1-10 of 14) with videos related to

Sort By:
Pageof 2
Ceskoslovenska Pediatrie|January 1, 1994
[Long-term therapy of true precocious puberty in girls using Decapetyl-Depot, a superactive gonadoliberin agonist in depot microcapsulated form]W G Sippell, C J Partsch, R Hümmelink, et al.
Monatsschrift Kinderheilkunde : Organ Der Deutschen Gesellschaft Fur Kinderheilkunde|May 1, 1989
[The significance and characteristics of the LHRH test in diagnosing precocious puberty development in girls: the stimulated LH/FSH quotient differentiates between central precocious puberty and premature thelarche]C J Partsch, R Hümmelink, F Lorenzen, et al.
The Journal of Clinical Endocrinology and Metabolism|February 1, 1979
"Acquired" adrenal hyperplasia with 21-hydroxylase deficiency is not the same genetic disorders as congenital adrenal hyperplasiaM I New, F Lorenzen, S Pang, et al.
Lancet (London, England)|June 2, 1990
Improved test to identify heterozygotes for congenital adrenal hyperplasia without index case examinationM Peter, W G Sippell, F Lorenzen, et al.
Military Medicine|May 1, 1993
A prototype multidisciplinary cancer screening clinic for the military medical facilityD W Johnson, J J Twidwell, R Henderson, et al.
Pediatric Research|December 1, 1979
Hormonal phenotype and HLA-genotype in families of patients with congenital adrenal hyperplasia (21-hydroxylase deficiency)F Lorenzen, S Pang, M I New, et al.
The Journal of Clinical Endocrinology and Metabolism|March 1, 1980
Hormonal studies in obligate heterozygotes and siblings of patients with 11 beta-hydroxylase deficiency congenital adrenal hyperplasiaS Pang, L S Levine, F Lorenzen, et al.
Prenatal Diagnosis|February 1, 1988
HLA-A,B,C,DR typing and 17-OHP determination for second trimester prenatal diagnosis of 21-hydroxylase deficient CAHH Grosse-Wilde, E Valentine-Thon, U Vögeler, et al.
The Journal of Clinical Endocrinology and Metabolism|November 1, 1982
Late-onset steroid 21-hydroxylase deficiency: a variant of classical congenital adrenal hyperplasiaB Kohn, L S Levine, M S Pollack, et al.
American Journal of Human Genetics|July 1, 1981
HLA linkage and B14, DR1, BfS haplotype association with the genes for late onset and cryptic 21-hydroxylase deficiencyM S Pollack, L S Levine, G J O'Neill, et al.
Pageof 2