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Results of search for 'au:"Reade, T"', page 1 of 2
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Authors
Clow, C
Clow, C L
Cole, D E
Costa, T
DeLuca, H F
Glorieux, F H
Goodyer, P
Goodyer, P R
Jequier, S
Kronick, J
Lemieux, B
Marie, P J
Nogrady, B
Reade, T
Reade, T M
Riedler, J
Robertson, C F
Schwartz, S
Scriver, C R
Shields, E D
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Adolescent
Adult
Alkaline Phosphatase
Calcium
Child
Child, Preschool
Female
Growth
Humans
Hydroxycholecalciferols
Hypophosphatemia, Familial
Infant
Kidney
Male
Phenotype
Phosphates
X Chromosome
administration & dosage
blood
therapeutic use
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English
Your search returned 29 results.
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1.
Sypilitic Affections of the Nervous System: A Retrospect.
[electronic resource]
by
Reade, T
Producer:
20110329
In:
British medical journal
vol. 2
Online resources:
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2.
Home care of children with inborn errors of metabolism.
[electronic resource]
by
Reade, T
Clow, C
Producer:
19701103
In:
The Canadian nurse
vol. 66
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3.
A healthy child, a sure future. A regional program for the management of hereditary metabolic disease.
[electronic resource]
by
Reade, T
Clow, C
Producer:
19800124
In:
The Canadian nurse
vol. 75
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4.
Hypophosphatemic rickets and breast milk.
[electronic resource]
by
Reade, T M
Scriver, C R
Producer:
19790728
In:
The New England journal of medicine
vol. 300
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5.
Renal hypophosphataemia has several mendelian forms.
[electronic resource]
by
Scriver, C R
Reade, T M
Producer:
19871117
In:
Lancet (London, England)
vol. 2
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6.
Repeatability of response to hypertonic saline aerosol in children with mild to severe asthma.
[electronic resource]
by
Riedler, J
Reade, T
Robertson, C F
Producer:
19950421
In:
Pediatric pulmonology
vol. 18
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7.
Management of hereditary metabolic disease. The role of allied health personnel.
[electronic resource]
by
Clow, C L
Reade, T M
Scriver, C R
Producer:
19710706
In:
The New England journal of medicine
vol. 284
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8.
Outcome of early and long-term management of classical maple syrup urine disease.
[electronic resource]
by
Clow, C L
Reade, T M
Scriver, C R
Producer:
19820313
In:
Pediatrics
vol. 68
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9.
Inhaled hypertonic saline increases sputum expectoration in cystic fibrosis.
[electronic resource]
by
Riedler, J
Reade, T
Button, B
Robertson, C F
Producer:
19960730
In:
Journal of paediatrics and child health
vol. 32
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10.
Prospective analysis and classification of patients with cystinuria identified in a newborn screening program.
[electronic resource]
by
Goodyer, P R
Clow, C
Reade, T
Girardin, C
Producer:
19930430
In:
The Journal of pediatrics
vol. 122
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11.
Audiometric evidence for two forms of X-linked hypophosphatemia in humans, apparent counterparts of Hyp and Gy mutations in mouse.
[electronic resource]
by
Boneh, A
Reade, T M
Scriver, C R
Rishikof, E
Producer:
19880128
In:
American journal of medical genetics
vol. 27
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12.
Renal ultrasound in metabolic bone disease.
[electronic resource]
by
Jequier, S
Cramer, B
Goodyer, P
Kronick, J
Reade, T
Producer:
19860401
In:
Pediatric radiology
vol. 16
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13.
Microencapsulated xanthine oxidase as experimental therapy in Lesch-Nyhan disease.
[electronic resource]
by
Palmour, R M
Goodyer, P
Reade, T
Chang, T M
Producer:
19891018
In:
Lancet (London, England)
vol. 2
Online resources:
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14.
Hypertonic saline challenge in an epidemiologic survey of asthma in children.
[electronic resource]
by
Riedler, J
Reade, T
Dalton, M
Holst, D
Robertson, C
Producer:
19941228
In:
American journal of respiratory and critical care medicine
vol. 150
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15.
Oral findings in patients with autosomal dominant hypophosphatemic bone disease and X-linked hypophosphatemia: further evidence that they are different diseases.
[electronic resource]
by
Schwartz, S
Scriver, C R
Reade, T M
Shields, E D
Producer:
19881123
In:
Oral surgery, oral medicine, and oral pathology
vol. 66
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16.
Hypophosphatemic nonrachitic bone disease: an entity distinct from X-linked hypophosphatemia in the renal defect, bone involvement, and inheritance.
[electronic resource]
by
Scriver, C R
MacDonald, W
Reade, T
Glorieux, R H
Nogrady, B
Producer:
19780517
In:
American journal of medical genetics
vol. 1
Online resources:
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17.
Autosomal hypophosphataemic bone disease responds to 1,25-(OH)2D3.
[electronic resource]
by
Scriver, C R
Reade, T
Halal, F
Costa, T
Cole, D E
Producer:
19810526
In:
Archives of disease in childhood
vol. 56
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18.
Vitamin D dependency: an inherited postnatal syndrome with secondary hyperparathyroidism.
[electronic resource]
by
Arnaud, C
Maijer, R
Reade, T
Scriver, C R
Whelan, D T
Producer:
19710223
In:
Pediatrics
vol. 46
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19.
Serum 1,25-dihydroxyvitamin D levels in normal subjects and in patients with hereditary rickets or bone disease.
[electronic resource]
by
Scriver, C R
Reade, T M
DeLuca, H F
Hamstra, A J
Producer:
19781202
In:
The New England journal of medicine
vol. 299
Online resources:
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20.
Use of phosphate and vitamin D to prevent dwarfism and rickets in X-linked hypophosphatemia.
[electronic resource]
by
Glorieux, F H
Scriver, C R
Reade, T M
Goldman, H
Roseborough, A
Producer:
19720922
In:
The New England journal of medicine
vol. 287
Online resources:
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