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Search Results - GRUMIERI, G
Search Results - GRUMIERI, G
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Mild fetal hydronephrosis indicating vesicoureteric reflux
by
Marra, G
,
Barbieri, G
,
Moioli, C
,
Assael, B M
,
Grumieri, G
,
Caccamo, M L
Published in
Archives of disease in childhood. Fetal and neonatal edition
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Renal tract ultrasonography and calcium homeostasis in Williams-Beuren syndrome
by
Sforzini, Cinzia
,
Milani, Donatella
,
Fossali, Emilio
,
Barbato, Anna
,
Grumieri, Gianpaolo
,
Bianchetti, Mario G
,
Selicorni, Angelo
Published in
Pediatric nephrology (Berlin, West)
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Phenotypic variability in Bartter syndrome type I
by
BETTINELLI, A
,
CIARMATORI, S
,
LEOZAPPA, G
,
BINDA, S
,
CECCONI, M
,
NAVONE, C
,
CURCIO, C
,
SYREN, M. L
,
CASARI, G
,
CESAREO, L
,
TEDESCHI, S
,
RUFFA, G
,
APPIANI, A. C
,
ROSINI, A
,
GRUMIERI, G
,
MERCURI, B
,
SACCO, M
Published in
Pediatric nephrology (Berlin, West)
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Mild fetal hydronephrosis indicating vesicoureteric reflux
by
Marra, G.
,
Barbieri, G.
,
Moioli, C.
,
Assael, B. M.
,
Grumieri, G.
,
Caccamo, M. L.
Published in
Pediatric nephrology (Berlin, West)
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Mild fetal hydronephrosis indicating vesicoureteric reflux. Commentary
by
MARRA, G
,
BARBIERI, G
,
MOIOLI, C
,
ASSAEL, B. M
,
GRUMIERI, G
,
CACCAMO, M. L
,
JONES, K. V
Published in
Archives of disease in childhood
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Pediatric Nephrology
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Archives Of Disease In Childhood
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Archives Of Disease In Childhood. Fetal And Neonatal Edition
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Biological And Medical Sciences
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Child
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Child, Preschool
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Hypercalciuria
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Infant
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Life Sciences & Biomedicine
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Pediatrics
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Amino Acid Sequence - Genetics
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Bartter Syndrome
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Bartter Syndrome - Genetics
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Bumetanide-Sensitive Cotransporter Gene
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Calcium - Blood
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