Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Robert G. McArthur"'
Publikováno v:
Clinical Genetics. 36:269-269
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::59c02aa1a13289a3ca805036ef08706e
https://doi.org/10.1111/j.1399-0004.1989.tb03202.x
https://doi.org/10.1111/j.1399-0004.1989.tb03202.x
Publikováno v:
Acta Paediatrica. 66:525-528
Triiodothyronine (T3) toxicity has been well documented in adults, but only isolated cases have been reported in children. Two girls presented with firm goitres and overt hyperthyroidism. In each patient, total serum thyroxine (T4) values by competit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db620adc855615db26390785eb4b2718
https://doi.org/10.1111/j.1651-2227.1977.tb07939.x
https://doi.org/10.1111/j.1651-2227.1977.tb07939.x
Autor:
John M. Opitz, Kenneth Morgan, John A. Phillips, John S. Klassen, James F. Reynolds, Marvin Bala, Robert G. McArthur
Publikováno v:
American Journal of Medical Genetics. 22:553-566
Familial hypopituitarism in the Hutterite Brethren is an autosomal recessive disorder involving sequential loss of anterior pituitary tropic hormones. Five individuals from two closely related families have been followed for 19 years. Both families a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9e2e90b5a4a0561f018e115bce5bc164
https://doi.org/10.1002/ajmg.1320220313
https://doi.org/10.1002/ajmg.1320220313
Autor:
Reginald S. Sauve, Douglas D. McMillan, Robert G. McArthur, Stuart A. Ross, Alexander K. C. Leung
Publikováno v:
The Journal of Pediatrics. 95:752-754
swelling because of the osmotic activity of intracellular galactitol. With a block in galactose metabolism due to defective galactokinase activity, there is little or no formation of galactose-l-phosphate, so that the formation of galactitol and its
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::98e67152a4d1feb59ae65eeb9dd1175d
https://doi.org/10.1016/s0022-3476(79)80730-1
https://doi.org/10.1016/s0022-3476(79)80730-1
Autor:
Karl Lederis, Alexander K. C. Leung, David Ko, John T. Parboosingh, Douglas D. McMillan, John S. R. Deacon, Robert G. McArthur
Publikováno v:
Acta paediatrica Scandinavica. 69(4)
Leung, A., McArthur, R., McMillan, D., Ko, D., Deacon, J., Parboosingh, J. and Lederis K. (the Divisions of Paediatrics, Pharmacology and Obstetrics, Faculty of Medicine, University of Calgary, Calgary, Alberta, Canada). Circulating antidiuretic horm
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3fb8873c3415c84c3994611edbab6e26
https://pubmed.ncbi.nlm.nih.gov/7446100
https://pubmed.ncbi.nlm.nih.gov/7446100
Publikováno v:
American journal of medical genetics. 32(1)
We describe a family with autosomal dominant hypoparathyroidism. The 3 affected individuals had no detectable serum parathyroid hormone on radioimmunoassay. The propositus presented with seizures and on CT scan had bilateral basal ganglion calcificat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad9a5ddd3fac96e245d4ec0213439cd3
https://pubmed.ncbi.nlm.nih.gov/2705481
https://pubmed.ncbi.nlm.nih.gov/2705481
Publikováno v:
The Journal of pediatrics. 95(2)
In view of the published reports of the successful correction of hypercortisolism in adult patients with Cushing disease by external pituitary irradiation and transsphenoidal pituitary microsurgery, leaving the patients with intact pituitary and adre
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::636185ded20eaa663f4ed90bc0373dce
https://pubmed.ncbi.nlm.nih.gov/448561
https://pubmed.ncbi.nlm.nih.gov/448561
Publikováno v:
Annals of plastic surgery. 15(2)
A male infant is reported in whom substantial gynecomastia resolved following removal of a giant pigmented nevus. Endocrinological studies were normal. It is postulated that the nevus contributed to the development of gynecomastia. Surgeons should be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1d2a6e2a06157368b7200d044b80c759
https://pubmed.ncbi.nlm.nih.gov/4091472
https://pubmed.ncbi.nlm.nih.gov/4091472
Autor:
Michael D. Whitaker, Morris Davidman, Bernard Corenblum, Robert H. Haslam, Robert G. McArthur
Publikováno v:
The American journal of medicine. 67(3)
A 15 year old girl presented with excessive thirst and hypertension (170110 mm Hg). Biochemical investigations revealed serum sodium 118 meq/liter, serum osmolality 238 mosmol/liter, urine sodium 90 meq/liter, urine osmolality 700 mosmol/liter, persi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ee892bc39eed55117d8df3209f096b1
https://pubmed.ncbi.nlm.nih.gov/474598
https://pubmed.ncbi.nlm.nih.gov/474598