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PubPharm (33)
1
β1-Integrin blockade prevents podocyte injury in experimental models of minimal change disease
enthalten in:
Nefrologia
| 2024
von
Cara-Fuentes, G.
|
Verma, R.
|
Venkatareddy, M.
| +12
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2
DECTIN-1 : A modifier protein in CTLA-4 haploinsufficiency
enthalten in:
Science advances
| 2023
von
Turnbull, C.
|
Bones, J.
|
Stanley, M.
| +23
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3
Hypercapnia in hospitalized children and adolescents with anorexia nervosa as a predictive marker for readmission : a prospective study
enthalten in:
Eating and weight disorders : EWD
| 2023
von
Viaño-Nogueira, P.
|
Aparicio-López, C.
|
Prieto-Campo, .
| +4
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4
The International X-Linked Hypophosphatemia (XLH) Registry : first interim analysis of baseline demographic, genetic and clinical data
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Ariceta, G.
|
Beck-Nielsen, S.
|
Boot, A.
| +17
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5
The International X-Linked Hypophosphatemia (XLH) Registry: first interim analysis of baseline demographic, genetic and clinical data
enthalten in:
Orphanet journal of rare diseases
| 2023
von
Ariceta, G.
|
Beck-Nielsen, S.
|
Boot, A.
| +17
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6
UMOD-related autosomal dominant tubulointerstitial kidney disease : an unfavourable novel mutation
enthalten in:
Nefrologia
| 2023
von
Viaño Nogueira, P.
|
de Lucas Collantes, C.
|
Ortiz Cabrera, V.
| +2
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7
Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.
enthalten in:
ResearchSquare.com
| 2022
von
Rodríguez-Rubio, E.
|
Gil-Peña, H.
|
Chocrón, S.
| +18
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8
Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.
enthalten in:
ResearchSquare.com
| 2022
von
Rodríguez-Rubio, E.
|
Gil-Peña, H.
|
Chocrón, S.
| +18
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9
Phenotypic characterization of X-linked hypophosphatemia in pediatric Spanish population.
enthalten in:
ResearchSquare.com
| 2022
von
Rodríguez-Rubio, E.
|
Gil-Peña, H.
|
Chocrón, S.
| +18
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10
TLR7 gain-of-function genetic variation causes human lupus
enthalten in:
Nature
| 2022
von
Brown, G.
|
Cañete, P.
|
Wang, H.
| +41
CommentIn: Nat Rev Rheumatol. 2022 Jul;18(7):365. - PMID 35610363
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8
Orphanet journal of rare diseases
3
Nefrologia
3
ResearchSquare.com
2
Anales de pediatria
2
Inflammatory bowel diseases
2
Nefrologia : publicacion oficial de la Sociedad...
1
Andes pediatrica : revista Chilena de pediatria
1
BMJ case reports
1
Clinical nutrition ESPEN
1
Eating and weight disorders : EWD
1
Frontiers in endocrinology
1
Frontiers in medicine
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Nature
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Thema
19
Journal Article
6
Case Reports
6
Letter
5
Research Support, Non-U.S. Gov't
4
Review
4
X-linked hypophosphatemia (XLH)
3
570
3
Biology
3
XLH
3
rickets
2
Bone deformities
2
EC 3.4.24.-
2
Fibroblast growth factor 23 (FGF23)
2
Growth retardation
2
Hypophosphatemic rickets
2
Inherited hypophosphatemia
2
International
2
Natural history
2
Observational Study
2
Osteomalacia
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Erscheinungszeitraum
24
2020-
9
2010-2019
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Sprache
32
Englisch
1
Spanisch
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