Sandra Wessman
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Explore the profile of Sandra Wessman including associated specialties, affiliations and a list of published articles.
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19
Citations
78
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Recent Articles
1.
Maya-Gonzalez C, Diaz De Stahl T, Wessman S, Taylan F, Tesi B, Lagerstedt-Robinson K, et al.
Am J Case Rep
. 2024 Dec;
25:e945715.
PMID: 39733240
BACKGROUND Limb-girdle muscular dystrophy recessive 1 (LGMDR1) is an autosomal recessive degenerative muscle disorder characterized by progressive muscular weakness caused by pathogenic variants in the CAPN3 gene. Desmoplastic small round...
2.
Park S, Fransson S, Sundquist F, Nilsson J, Gryback P, Wessman S, et al.
Front Oncol
. 2024 Sep;
14:1408729.
PMID: 39324010
In this case report, we present the treatment outcomes of the first patient enrolled in the LuDO-N trial. The patient is a 21-month-old girl diagnosed with high-risk neuroblastoma (NB) and...
3.
Maya-Gonzalez C, Delgado-Vega A, Taylan F, Lagerstedt Robinson K, Hansson L, Pal N, et al.
Am J Med Genet A
. 2024 Jul;
194(12):e63812.
PMID: 38990105
Marfan syndrome (MFS) is an autosomal dominant connective tissue disorder caused by pathogenic variants in FBN1, with a hitherto unknown association with cancer. Here, we present two females with MFS...
4.
Tesi B, Lagerstedt Robinson K, Abel F, Diaz De Stahl T, Orrsjo S, Poluha A, et al.
Lancet Reg Health Eur
. 2024 May;
39:100881.
PMID: 38803632
Background: Childhood cancer predisposition (ChiCaP) syndromes are increasingly recognized as contributing factors to childhood cancer development. Yet, due to variable availability of germline testing, many children with ChiCaP might go...
5.
Bartosch C, Nadal A, Braga A, Salerno A, Rougemont A, Van Rompuy A, et al.
Virchows Arch
. 2024 Feb;
484(3):539-548.
PMID: 38421406
No abstract available.
6.
Wessman S, Nister M, Kokaraki G, Pal N, Tettamanti G, Petta T, et al.
Gynecol Oncol
. 2024 Feb;
184:206-213.
PMID: 38340646
Objectives: Ovarian tumors in the pediatric population are rare. The incidence and frequency of subtypes differ between children and adults. Although not all tumors are aggressive, they may still lead...
7.
Bartosch C, Nadal A, Braga A, Salerno A, Rougemont A, Van Rompuy A, et al.
Virchows Arch
. 2023 Oct;
484(3):401-422.
PMID: 37857997
Hydatidiform moles are rare and thus most pathologists and geneticists have little experience with their diagnosis. It is important to promptly and correctly identify hydatidiform moles given that they are...
8.
Maya-Gonzalez C, Wessman S, Lagerstedt-Robinson K, Taylan F, Tesi B, Kuchinskaya E, et al.
Front Med (Lausanne)
. 2023 Aug;
10:1172565.
PMID: 37575996
Prader-Willi syndrome (PWS) is a rare disease caused by a lack of expression of inherited imprinted genes in the paternally derived Prader-Willi critical region on chromosome 15q11.2-q13. It is characterized...
9.
Diagnostic Yield From a Nationwide Implementation of Precision Medicine for all Children With Cancer
Wadensten E, Wessman S, Abel F, Diaz De Stahl T, Tesi B, Pietras C, et al.
JCO Precis Oncol
. 2023 Jun;
7:e2300039.
PMID: 37384868
Purpose: Several studies have indicated that broad genomic characterization of childhood cancer provides diagnostically and/or therapeutically relevant information in selected high-risk cases. However, the extent to which such characterization offers...
10.
Wessman S, Fuentes B, Severin-Karlsson J, Westbom-Fremer S, Nister M, Kokaraki G, et al.
Int J Gynecol Pathol
. 2023 May;
43(1):78-89.
PMID: 37255476
Granulosa-cell tumors (GCTs) are the most common type of malignant ovarian sex cord-stromal tumor (SCST). The histopathologic diagnosis of these tumors can be challenging. A recurrent somatic mutation of the...