Detalhe da pesquisa
1.
Magnetic resonance T2 mapping and diffusion-weighted imaging for early detection of cystogenesis and response to therapy in a mouse model of polycystic kidney disease.
Kidney Int
; 92(6): 1544-1554, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-28754558
2.
Challenges in establishing genotype-phenotype correlations in ARPKD: case report on a toddler with two severe PKHD1 mutations.
Pediatr Nephrol
; 32(7): 1269-1273, 2017 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-28364132
3.
Mutations in WNT1 cause different forms of bone fragility.
Am J Hum Genet
; 92(4): 565-74, 2013 Apr 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-23499309
4.
Arterial Hypertension in a 10-Year-Old Girl.
Am J Kidney Dis
; 77(3): A11-A13, 2021 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-33618821
5.
Comparison of DXA Scans and Conventional X-rays for Spine Morphometry and Bone Age Determination in Children.
J Clin Densitom
; 19(2): 208-15, 2016.
Artigo
em Inglês
| MEDLINE | ID: mdl-26059565
6.
The pericardial reflection and the tip of the central venous catheter - topographical analysis in stillborn babies.
Pediatr Radiol
; 46(11): 1528-31, 2016 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-27350379
7.
A mutation in the 5'-UTR of IFITM5 creates an in-frame start codon and causes autosomal-dominant osteogenesis imperfecta type V with hyperplastic callus.
Am J Hum Genet
; 91(2): 349-57, 2012 Aug 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-22863195
8.
Mutation of POC1B in a severe syndromic retinal ciliopathy.
Hum Mutat
; 35(10): 1153-62, 2014 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-25044745
9.
Exome sequencing identifies truncating mutations in human SERPINF1 in autosomal-recessive osteogenesis imperfecta.
Am J Hum Genet
; 88(3): 362-71, 2011 Mar 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-21353196
10.
Pediatric computed tomography doses in Germany from 2016 to 2018 based on large-scale data collection.
Eur J Radiol
; 163: 110832, 2023 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-37059005
11.
Liver cell transplantation in severe infantile oxalosis--a potential bridging procedure to orthotopic liver transplantation?
Nephrol Dial Transplant
; 27(7): 2984-9, 2012 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-22287658
12.
Massive macroglossia after palatoplasty: case report and review of the literature.
Eur J Pediatr
; 171(3): 433-7, 2012 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-21912891
13.
Efficacy and Feasibility of Proton Beam Therapy in Relapsed High-Risk Neuroblastoma-Experiences from the Prospective KiProReg Registry.
Curr Oncol
; 29(11): 8222-8234, 2022 10 30.
Artigo
em Inglês
| MEDLINE | ID: mdl-36354709
14.
Finding alternative sites for intraosseous infusions in newborns.
Resuscitation
; 163: 57-63, 2021 Apr 20.
Artigo
em Inglês
| MEDLINE | ID: mdl-33862177
15.
PNPT1 mutations may cause Aicardi-Goutières-Syndrome.
Brain Dev
; 43(2): 320-324, 2021 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-33158637
16.
Proton Beam Therapy for Children With Neuroblastoma: Experiences From the Prospective KiProReg Registry.
Front Oncol
; 10: 617506, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33552991
17.
Work and Training Conditions of German Residents in Radiology - Results from a Nationwide Survey Conducted by the Young Radiology Forum in the German Roentgen Society. / Arbeits- und Weiterbildungsbedingungen in der Facharztweiterbildung Radiologie Ergebnisse einer bundesweiten Weiterbildungsumfrage durch das Forum Junge Radiologie in der Deutschen Röntgengesellschaft.
Rofo
; 192(5): 458-470, 2020 May.
Artigo
em Inglês, Alemão
| MEDLINE | ID: mdl-31918440
18.
Anatomical investigations on intraosseous access in stillborns - Comparison of different devices and techniques.
Resuscitation
; 127: 79-82, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29627398
19.
A novel mutation in sphingosine-1-phosphate lyase causing congenital brain malformation.
Brain Dev
; 40(6): 480-483, 2018 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-29501407
20.
[Challenges in Pediatric Radiology - Strategies of the board of the German speaking Society of Pediatric Radiology]. / Entwicklung der Kinder- und Jugendradiologie Strategiepapier des Vorstands der Gesellschaft für Pädiatrische Radiologie (GPR e.âV.).
Rofo
; 192(6): 531-536, 2020 Jun.
Artigo
em Alemão
| MEDLINE | ID: mdl-32074630