Zobrazeno 1 - 10
of 52
pro vyhledávání: '"Sang Whay Kooh"'
Publikováno v:
Clinical Endocrinology. 58:163-168
Summary objective X-linked hypophosphatemic rickets is characterized by renal phosphate wasting, hypophosphatemia and defective bone mineralization. Treatment with oral phosphate (Pi) and calcitriol improves skeletal changes but associates with secon
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::09b5d9cee9461c635e29bd4d04919943
https://doi.org/10.1046/j.1365-2265.2003.01685.x
https://doi.org/10.1046/j.1365-2265.2003.01685.x
Autor:
Alan Daneman, Etienne Sochett, Outi Mäkitie, Paul S. Thorner, Carol Huang, Sang Whay Kooh, Andrea S. Doria
Publikováno v:
Pediatric Radiology. 32:684-689
Neonatal primary hyperparathyroidism is a rare entity characterized by marked hypercalcemia, diffuse parathyroid hyperplasia, and skeletal demineralization. It is often lethal unless total parathyroidectomy is performed. Long-term outcome of treated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::483f07b276a33ab7be8d7b2616fd5a69
https://doi.org/10.1007/s00247-002-0737-0
https://doi.org/10.1007/s00247-002-0737-0
Publikováno v:
Pediatric Radiology. 29:68-72
Background. Nephrocalcinosis is often associated with a variety of hypercalcemic conditions. Diagnostic ultrasound is often used for assessing nephrocalcinosis in children, but its reliability has not been proven. Objective. To determine the reliabil
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::311fcf6bbe0c89da2fc9d9b6434ad731
https://doi.org/10.1007/s002470050539
https://doi.org/10.1007/s002470050539
Publikováno v:
Pediatric Nephrology. 11:633-636
Renal tubular acidosis with osteopetrosis is an autosomal recessive disorder due to deficiency of carbonic anhydrase II (CAII). A 3.5-year-old Egyptian boy with osteopetrosis and cerebral calcification had a persistent normal anion gap type of metabo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::366efa9a8890ca806fd82309dba3481b
https://doi.org/10.1007/s004670050354
https://doi.org/10.1007/s004670050354
Publikováno v:
Kidney International. 38(5):857-861
Tracer kinetics and actions of oral and intraperitoneal 1,25-dihydroxy-vitamin D 3 administration in rats. Tracer kinetic parameters of [ 3 H]-1,25(OH) 2 D 3 were calculated from data obtained following its acute oral (p.o.) or intraperitoneal (i.p.)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::184d6a5d0a1df987e35f654cb988dc05
Autor:
Andrea S. Doria, Outi Mäkitie, William G. Cole, Alan Daneman, Etienne Sochett, Sang Whay Kooh
Publikováno v:
The Journal of clinical endocrinology and metabolism. 88(8)
X-Linked hypophosphatemic rickets (XLH) is characterized by hypophosphatemia, rickets, and impaired growth. Despite oral phosphate and 1,25-dihydroxyvitamin D3 treatment, many patients have suboptimal growth and bone healing. The aim of this study wa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23bdf016711cb9b588cf343350feb574
https://pubmed.ncbi.nlm.nih.gov/12915641
https://pubmed.ncbi.nlm.nih.gov/12915641
Autor:
Flavia Henriques, Outi Mäkitie, Andrea S. Doria, Alan Daneman, Sang Whay Kooh, Etienne Sochett
Publikováno v:
Karolinska Institutet
Objective: X-linked hypophosphataemic rickets (XLH) results in defective bone mineralization and impaired growth. Treatment with oral phosphate (Pi) and calcitriol improves but does not normalize growth. This study assessed whether pubertal growth an
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9325e4961f347466a05b9c35c11bce47
https://pubmed.ncbi.nlm.nih.gov/15031616
https://pubmed.ncbi.nlm.nih.gov/15031616
Publikováno v:
European journal of pediatrics. 159(1-2)
Primary infantile hypomagnesaemia is an infrequent cause of neonatal hypocalcaemic seizures but one that responds well to magnesium supplementation. We describe a 22-year-old male, first reported at 4 months of age, who is currently free of neurologi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4628912f792ec26f33f072ec4edf1a64
https://pubmed.ncbi.nlm.nih.gov/10653327
https://pubmed.ncbi.nlm.nih.gov/10653327
Publikováno v:
Pediatric radiology. 28(9)
Medullary nephrocalcinosis (MNC) is usually a bilateral process with symmetric involvement of both kidneys. Asymmetric medullary nephrocalcinosis has been previously reported in the literature, but has not been well illustrated or explained. We repor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c8e650ba136412452e3ee83895c1333e
https://pubmed.ncbi.nlm.nih.gov/9732494
https://pubmed.ncbi.nlm.nih.gov/9732494
Autor:
Kamel S. Kamel, Sang Whay Kooh, J. Williamson Balfe, Peter D. Yorgin, Luis F. Briceno, Marta I. Sanchez, Mitchell L. Halperin, Luis Brenes
Publikováno v:
American journal of kidney diseases : the official journal of the National Kidney Foundation. 29(1)
The traditional classification of the group of disorders called renal tubular acidosis (RTA) into proximal and distal subclasses is based on which nephron segment is thought to have an abnormal function. Nevertheless, such a distinction may not be co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::84e698098f6bb5c298969e2e51681012
https://pubmed.ncbi.nlm.nih.gov/9002543
https://pubmed.ncbi.nlm.nih.gov/9002543