Trinh Hermanns‐Lê - Publications, H-index & Citations

Trinh Hermanns‐Lê

nottingham university hospital nhs trust

24H指数

211论文数

2.1K被引数

收录论文 20

发表时间

Caffey disease is associated with distinct arginine to cysteine substitutions in the proα1(I) chain of type I procollagen

GENETICS IN MEDICINE

IF6.2

2021-12-01

OAAI

Dhooge, Tibbe; Syx, Delfien; Hermanns-Le, Trinh; Hausser, Ingrid; Mortier, Geert; Zonana, Jonathan; Symoens, Sofie; Byers, Peter H.; Malfait, Fransiska

Hedgehog- and mTOR-targeted therapies for advanced basal cell carcinomas

FUTURE ONCOLOGY

IF2.6

2015-10-05

PREAI

Pierard-Franchimont, Claudine; Hermanns-Le, Trinh; Paquet, Philippe; Herfs, Michael; Delvenne, Philippe; Pierard, Gerald E.

Genetic Heterogeneity and Clinical Variability in Musculocontractural Ehlers-Danlos Syndrome Caused by Impaired Dermatan Sulfate Biosynthesis 硫酸皮肤素生物合成受损引起的肌肉收缩ehlers-danlos综合征的遗传异质性和临床变异性

HUMAN MUTATION

IF3.7

2015-04-06

PREAI

Syx, Delfien; Van Damme, Tim; Symoens, Sofie; Maiburg, Merel C.; van de Laar, Ingrid; Morton, Jenny; Suri, Mohnish; Del Campo, Miguel; Hausser, Ingrid; Hermanns-Le, Trinh; De Paepe, Anne; Malfait, Fransiska

Defective Proteolytic Processing of Fibrillar Procollagens and Prodecorin Due to Biallelic BMP1 Mutations Results in a Severe, Progressive Form of Osteogenesis Imperfecta 由于双等位基因BMP1突变导致的纤维状前胶原和Prodecorin的蛋白水解加工缺陷导致严重的进行性成骨不全

JOURNAL OF BONE AND MINERAL RESEARCH

IF5.9

2015-02-06

OAAI

Syx, Delfien; Guillemyn, Brecht; Symoens, Sofie; Sousa, Ana Berta; Medeira, Ana; Whiteford, Margo; Hermanns-Le, Trinh; Coucke, Paul J.; De Paepe, Anne; Malfait, Fransiska

Recent advances in toxicological testing of the stratum corneum

BRITISH JOURNAL OF DERMATOLOGY

IF9.6

2014-09-18

OAAI

Pierard, G. E.; Pierard-Franchimont, C.; Hermanns-Le, T.; Paquet, P.

Characterization of spontaneous collagen fibrillogenesis in a cell-free and tension-free environment

CLINICAL AND EXPERIMENTAL DERMATOLOGY

IF2.8

2013-03-27

PREAI

Pierard, G. E.; Hermanns-Le, T.; Delvenne, P.; Pierard-Franchimont, C.

Hypomelanosis of Ito: pigmentary mosaicism with immature melanosome in keratinocytes

INTERNATIONAL JOURNAL OF DERMATOLOGY

IF3.2

2011-09-25

PREAI

Devillers, Celine; Quatresooz, Pascale; Hermanns-Le, Trinh; Szepetiuk, Gregory; Lemaire, Roland; Pierard-Franchimont, Claudine; Pierard, Gerald E.

Musculocontractural Ehlers-Danlos Syndrome (Former EDS Type VIB) and Adducted Thumb Clubfoot Syndrome (ATCS) Represent a Single Clinical Entity Caused by Mutations in the Dermatan-4-sulfotransferase 1 Encoding CHST14 Gene

HUMAN MUTATION

IF3.7

2010-10-28

OAAI

Malfait, Fransiska; Syx, Delfien; Vlummens, Philip; Symoens, Sofie; Nampoothiri, Sheela; Hermanns-Le, Trinh; Van Laer, Lut; De Paepe, Anne

The RIN2 syndrome: a new autosomal recessive connective tissue disorder caused by deficiency of Ras and Rab interactor 2 (RIN2)

HUMAN GENETICS

IF3.6

2010-04-28

PREAI

Syx, Delfien; Malfait, Fransiska; Van Laer, Lut; Hellemans, Jan; Hermanns-Le, Trinh; Willaert, Andy; Benmansour, Abdelmajid; De Paepe, Anne; Verloes, Alain

Three arginine to cysteine substitutions 4 in the pro-alpha (I)-collagen chain cause Ehlers-Danlos syndrome with a propensity to arterial rupture in early adulthood

HUMAN MUTATION

IF3.7

2007-01-01

121

OAAI

Malfait, Fransiska; Symoens, Sofie; De Backer, Julie; Hermanns-Le, Trinh; Sakalihasan, Natzi; Lapiere, Charles M.; Coucke, Paul; De Paepe, Anne

Tensegrity and type 1 dermal dendrocytes in acromegaly

EUROPEAN JOURNAL OF CLINICAL INVESTIGATION

IF3.6

2005-01-24

PREAI