Detalhe da pesquisa
1.
[SARS-CoV-2 Infection in Pregnancy and Incidence of Congenital Malformations - is there a Correlation? Analysis of 8032 Pregnancies from the CRONOS Registry]. / SARS-CoV-2-Infektion in der Schwangerschaft und Auftreten von angeborenen Fehlbildungen Besteht ein Zusammenhang? Auswertung von 8032 Schwangerschaften aus dem CRONOS-Register.
Z Geburtshilfe Neonatol
; 228(1): 65-73, 2024 Feb.
Artigo
em Alemão
| MEDLINE | ID: mdl-38330961
2.
Epidemiology of inherited epidermolysis bullosa in Germany.
J Eur Acad Dermatol Venereol
; 37(2): 402-410, 2023 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-36196047
3.
A Causal Treatment for X-Linked Hypohidrotic Ectodermal Dysplasia: Long-Term Results of Short-Term Perinatal Ectodysplasin A1 Replacement.
Int J Mol Sci
; 24(8)2023 Apr 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-37108325
4.
A surrogate cell-based SARS-CoV-2 spike blocking assay.
Eur J Immunol
; 51(11): 2665-2676, 2021 11.
Artigo
em Inglês
| MEDLINE | ID: mdl-34547822
5.
Unbound Corneocyte Lipid Envelopes in 12R-Lipoxygenase Deficiency Support a Specific Role in Lipid-Protein Cross-Linking.
Am J Pathol
; 191(5): 921-929, 2021 05.
Artigo
em Inglês
| MEDLINE | ID: mdl-33607042
6.
Maternal SARS-CoV-2 infection during pregnancy: possible impact on the infant.
Eur J Pediatr
; 181(1): 413-418, 2022 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-34355278
7.
Ectodysplasin A1 Deficiency Leads to Osteopetrosis-like Changes in Bones of the Skull Associated with Diminished Osteoclastic Activity.
Int J Mol Sci
; 23(20)2022 Oct 13.
Artigo
em Inglês
| MEDLINE | ID: mdl-36293046
8.
Deficiency of Fhl2 leads to delayed neuronal cell migration and premature astrocyte differentiation.
J Cell Sci
; 132(6)2019 03 18.
Artigo
em Inglês
| MEDLINE | ID: mdl-30745335
9.
Prenatal Correction of X-Linked Hypohidrotic Ectodermal Dysplasia.
N Engl J Med
; 378(17): 1604-1610, 2018 04 26.
Artigo
em Inglês
| MEDLINE | ID: mdl-29694819
10.
T Cell Impairment Is Predictive for a Severe Clinical Course in NEMO Deficiency.
J Clin Immunol
; 40(3): 421-434, 2020 04.
Artigo
em Inglês
| MEDLINE | ID: mdl-31965418
11.
Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects.
Br J Clin Pharmacol
; 86(10): 2063-2069, 2020 10.
Artigo
em Inglês
| MEDLINE | ID: mdl-32250462
12.
Prenatal Treatment of X-Linked Hypohidrotic Ectodermal Dysplasia using Recombinant Ectodysplasin in a Canine Model.
J Pharmacol Exp Ther
; 370(3): 806-813, 2019 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-31000577
13.
Variants of the ectodysplasin A1 receptor gene underlying homozygous cases of autosomal recessive hypohidrotic ectodermal dysplasia.
Clin Genet
; 95(3): 427-432, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30623979
14.
Ectodermal dysplasias: Classification and organization by phenotype, genotype and molecular pathway.
Am J Med Genet A
; 179(3): 442-447, 2019 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-30703280
15.
Attenuation of Severe Generalized Junctional Epidermolysis Bullosa by Systemic Treatment with Gentamicin.
Dermatology
; 235(4): 315-322, 2019.
Artigo
em Inglês
| MEDLINE | ID: mdl-31132778
16.
Reliability of prenatal detection of X-linked hypohidrotic ectodermal dysplasia by tooth germ sonography.
Prenat Diagn
; 39(9): 796-805, 2019 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-30394555
17.
Attenuation of Mammary Gland Dysplasia and Feeding Difficulties in Tabby Mice by Fetal Therapy.
J Mammary Gland Biol Neoplasia
; 23(3): 125-138, 2018 09.
Artigo
em Inglês
| MEDLINE | ID: mdl-29855766
18.
Sweating ability of patients with p63-associated syndromes.
Eur J Pediatr
; 177(11): 1727-1731, 2018 Nov.
Artigo
em Inglês
| MEDLINE | ID: mdl-30088137
19.
Automatic recognition of the XLHED phenotype from facial images.
Am J Med Genet A
; 173(9): 2408-2414, 2017 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-28691769
20.
Increased Rat Placental Fatty Acid, but Decreased Amino Acid and Glucose Transporters Potentially Modify Intrauterine Programming.
J Cell Biochem
; 117(7): 1594-603, 2016 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-26590355