acid-phosphatase and Adrenal-Insufficiency

acid-phosphatase has been researched along with Adrenal-Insufficiency* in 2 studies

Other Studies

2 other study(ies) available for acid-phosphatase and Adrenal-Insufficiency

Article	Year
Biological parameters of bone remodelling in chronic adrenal insufficiency. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 1991, Volume: 23, Issue:10 Topics: Acid Phosphatase; Adrenal Insufficiency; Bone Remodeling; Calcium; Creatinine; Female; Humans; Hydrocortisone; Hydroxyproline; Middle Aged; Tartrates	1991
Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome. American journal of medical genetics, 1988, Volume: 29, Issue:3 We have studied patients with Duchenne muscular dystrophy (DMD), DMD together with glycerol kinase (GK) deficiency, or DMD together with both GK deficiency and congenital adrenal hypoplasia (AHC). Analysis of deletions in these patients allows the mapping of these mutations in Xp21. The following order is proposed: Xpter - L1 - AHC - GK - DMD - Xcen. One of the boys with DMD, GK, and AHC is shown by pulsed-field-gel electrophoresis to have a deletion which has a proximal endpoint at least 500 kb distal from the pERT87 (DXS164) locus. Topics: Acid Phosphatase; Adrenal Insufficiency; Cell Line; Child; Child, Preschool; Chromosome Deletion; Chromosome Mapping; DNA; Glycerol Kinase; Humans; Male; Phosphotransferases; Sex Chromosome Aberrations; X Chromosome	1988

Article

Year

Biological parameters of bone remodelling in chronic adrenal insufficiency.

Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme, 1991, Volume: 23, Issue:10

Topics: Acid Phosphatase; Adrenal Insufficiency; Bone Remodeling; Calcium; Creatinine; Female; Humans; Hydrocortisone; Hydroxyproline; Middle Aged; Tartrates

1991

Fine mapping of glycerol kinase deficiency and congenital adrenal hypoplasia within Xp21 on the short arm of the human X chromosome.

American journal of medical genetics, 1988, Volume: 29, Issue:3

We have studied patients with Duchenne muscular dystrophy (DMD), DMD together with glycerol kinase (GK) deficiency, or DMD together with both GK deficiency and congenital adrenal hypoplasia (AHC). Analysis of deletions in these patients allows the mapping of these mutations in Xp21. The following order is proposed: Xpter - L1 - AHC - GK - DMD - Xcen. One of the boys with DMD, GK, and AHC is shown by pulsed-field-gel electrophoresis to have a deletion which has a proximal endpoint at least 500 kb distal from the pERT87 (DXS164) locus.

Topics: Acid Phosphatase; Adrenal Insufficiency; Cell Line; Child; Child, Preschool; Chromosome Deletion; Chromosome Mapping; DNA; Glycerol Kinase; Humans; Male; Phosphotransferases; Sex Chromosome Aberrations; X Chromosome

1988