Caroline Kannengiesser
Overview
Explore the profile of Caroline Kannengiesser including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
Snapshot
Snapshot
Articles
126
Citations
2547
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
1.
Manali E, Griese M, Nathan N, Uzunhan Y, Borie R, Michel K, et al.
Eur Respir J
. 2024 Dec;
65(2).
PMID: 39638417
Background: Interstitial lung disease is rarer in children than adults, but, with increasing diagnostic awareness, more cases are being discovered. The prognosis of childhood interstitial lung disease is often poor,...
2.
Borie R, Berteloot L, Kannengiesser C, Griese M, Cazes A, Crestani B, et al.
Eur Respir Rev
. 2024 Nov;
33(174).
PMID: 39537246
The main monogenic causes of pulmonary fibrosis in adults are mutations in telomere-related genes. These mutations may be associated with extrapulmonary signs (hepatic, haematological and dermatological) and typically present radiologically...
3.
Raynor A, Peoch K, Boi C, Manceau H, Pissard S, Diallo K, et al.
Blood Cells Mol Dis
. 2024 Nov;
110:102898.
PMID: 39531753
Congenital microcytic anemias are rare diseases associated with decreased hemoglobin synthesis and red blood cells of low corpuscular volume. DMT1/NRAMP2 is a highly conserved divalent cation transporter encoded by the...
4.
Maillet F, Galimard J, Borie R, Lainey E, Larcher L, Passet M, et al.
Br J Haematol
. 2024 Sep;
205(5):1835-1847.
PMID: 39279213
Data on haematological features of telomere biology disorders (TBD) remain scarce. We describe haematological, extra-haematological characteristics and prognosis of 127 genetically confirmed TBD patients diagnosed after the age of 15....
5.
Kochman R, Ba I, Yates M, Pirabakaran V, Gourmelon F, Churikov D, et al.
Genes Dev
. 2024 Sep;
38(15-16):755-771.
PMID: 39231615
Premature telomere shortening or telomere instability is associated with a group of rare and heterogeneous diseases collectively known as telomere biology disorders (TBDs). Here we identified two unrelated individuals with...
6.
Hussein-Agha R, Kannengiesser C, Lainey E, Marcais A, Srour M, Sterin A, et al.
Bone Marrow Transplant
. 2024 Jul;
59(10):1428-1432.
PMID: 39080469
While HSCT is the only curative option for patients with short telomere syndromes (STSs) and severe bone marrow failure (BMF) or myeloid malignancies (MM), their increase sensitivity to conditioning regimen...
7.
Borie R, Ba I, Debray M, Kannengiesser C, Crestani B
Curr Opin Pulm Med
. 2024 Jun;
30(5):473-483.
PMID: 38896087
Purpose Of Review: The identification of extra-pulmonary symptoms plays a crucial role in diagnosing interstitial lung disease (ILD). These symptoms not only indicate autoimmune diseases but also hint at potential...
8.
Juge P, Sparks J, Gazal S, Ebstein E, Borie R, Debray M, et al.
Rheumatol Adv Pract
. 2024 Jun;
8(2):rkae059.
PMID: 38854416
Objective: Recently, a genome-wide association study identified an association between RA-associated interstitial lung disease (ILD) and rs12702634 in the Japanese population, especially for patients with a usual interstitial pneumonia (UIP)...
9.
Hercent A, Bennani R, Lafitte P, Mary M, Lamoril J, Bourrat E, et al.
Clin Exp Dermatol
. 2024 May;
50(2):380-386.
PMID: 38768301
Background: Gorlin syndrome (GS) is an autosomal dominant disorder characterized by a predisposition to basal cell carcinoma and developmental defects. It is caused by pathogenic variants in the PTCH1 or...
10.
Brudon A, Legendre M, Mageau A, Bermudez J, Bonniaud P, Bouvry D, et al.
Eur Respir J
. 2024 Apr;
63(5).
PMID: 38575158
Background: Several rare surfactant-related gene (SRG) variants associated with interstitial lung disease are suspected to be associated with lung cancer, but data are missing. We aimed to study the epidemiology...