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مکتبة رقمیه للعلوم الطبيه
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Results of search for 'au:"Al-Abbad, A"'
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Authors
Al Abbad, A
Al Sabban, E
Al Shorafa, S
Al-Abbad, A
Al-Abbad, A J
Al-Sabban, E
Bella, H
Burwinkel, B
Cabral, D A
Ibrahim, A
Khauli, R B
Kilimann, M W
LeQuesne, G
Malleson, P N
Nazer, H
Petty, R E
Sanatani, S
Sandor, G G
Sanjad, S A
al-Abbad, A
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Topics
Acidosis
Adolescent
Age Factors
Amino Acid Sequence
Amino Acid Substitution
Base Sequence
Cadaver
Causality
Child
Child, Preschool
Consanguinity
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Humans
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blood
complications
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English
Your search returned 9 results.
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1.
Diarrhoea in the under-fives in a Saudi semiurban community.
[electronic resource]
by
al-Abbad, A A
Bella, H
Producer:
19910409
In:
Tropical and geographical medicine
vol. 42
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No items available.
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2.
Primary hyperoxaluria type 1: An underestimated cause of nephrocalcinosis and chronic renal failure in Saudi Arabian children.
[electronic resource]
by
Sanjad, S A
Al-Abbad, A
Al-Sabban, E
Producer:
20121002
In:
Annals of Saudi medicine
vol. 19
Online resources:
Available from publisher's website
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3.
Management of hyperlipidemia in children with refractory nephrotic syndrome: the effect of statin therapy.
[electronic resource]
by
Sanjad, S A
al-Abbad, A
al-Shorafa, S
Producer:
19970408
In:
The Journal of pediatrics
vol. 130
Online resources:
Available from publisher's website
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4.
Congenital chloride diarrhea: A single center experience with ten patients.
[electronic resource]
by
Al-Abbad, A
Nazer, H
Sanjad, S A
Al-Sabban, E
Producer:
20121002
In:
Annals of Saudi medicine
vol. 15
Online resources:
Available from publisher's website
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5.
Congenital rickets secondary to untreated maternal renal failure.
[electronic resource]
by
al-Senan, K
al-Alaiyan, S
al-Abbad, A
LeQuesne, G
Producer:
20020405
In:
Journal of perinatology : official journal of the California Perinatal Association
vol. 21
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6.
Apparent medium vessel vasculitis associated with a spinal meningioma.
[electronic resource]
by
Al-Abbad, A J
Malleson, P N
Petty, R E
Cabral, D A
Producer:
19990630
In:
The Journal of rheumatology
vol. 26
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7.
A mutation in GLUT2, not in phosphorylase kinase subunits, in hepato-renal glycogenosis with Fanconi syndrome and low phosphorylase kinase activity.
[electronic resource]
by
Burwinkel, B
Sanjad, S A
Al-Sabban, E
Al-Abbad, A
Kilimann, M W
Producer:
20000918
In:
Human genetics
vol. 105
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8.
Renal tubular dysfunction following kidney transplantation: a prospective study in 31 children.
[electronic resource]
by
Sanjad, S A
Ibrahim, A
Al Shorafa, S
Al Abbad, A
Khauli, R B
Shaibani, K A
Al Sabban, E
Producer:
20011204
In:
Transplantation proceedings
vol. 33
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9.
Echocardiography and pulmonary function testing in childhood onset systemic lupus erythematosus.
[electronic resource]
by
Al-Abbad, A J
Cabral, D A
Sanatani, S
Sandor, G G
Seear, M
Petty, R E
Malleson, P N
Producer:
20010614
In:
Lupus
vol. 10
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