Carole Gengler

Lausanne, VD, Switzerland

Last Updated: 09/26/2026

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Found 22 publications

Case Report: A novel approach to prevent chronic histiocytic intervillositis and recurrent pregnancy loss by targeting maternal alloimmunity.

Case Report: A novel approach to prevent chronic histiocytic intervillositis and recurrent pregnancy loss by targeting maternal alloimmunity.

Journal: Frontiers in immunology
Published: August 26, 2025

Ultrasound and magnetic resonance imaging of fetal gastrointestinal tract disorders.

Ultrasound and magnetic resonance imaging of fetal gastrointestinal tract disorders.

Journal: Abdominal radiology (New York)
Published: July 04, 2025

An update on the pathology of peripheral neuroblastic tumors

An update on the pathology of peripheral neuroblastic tumors

Journal: Annales de pathologie
Published: March 11, 2025

Severe Neonatal Anemia with Multi-Organ Failure, Extreme Placentomegaly, and Placental Megaloblastic Erythroblastosis as Features in Identifying Congenital Dyserythropoietic Anemia Type 1: A Case Report.

Severe Neonatal Anemia with Multi-Organ Failure, Extreme Placentomegaly, and Placental Megaloblastic Erythroblastosis as Features in Identifying Congenital Dyserythropoietic Anemia Type 1: A Case Report.

Journal: Neonatology
Published: February 26, 2025

Symmetrical Thalamic Lesions in Preterm Triplets: What Can We Learn From the Different Phenotypes?

Symmetrical Thalamic Lesions in Preterm Triplets: What Can We Learn From the Different Phenotypes?

Journal: Pediatric neurology
Published: January 23, 2025

Managing High-Risk PTPN11-Mutated Juvenile Myelomonocytic Leukemia in a Patient with SETBP1 Mosaicism.

Managing High-Risk PTPN11-Mutated Juvenile Myelomonocytic Leukemia in a Patient with SETBP1 Mosaicism.

Journal: Pediatric blood & cancer
Published: November 25, 2024

ENT manifestations of myeloid sarcoma

ENT manifestations of myeloid sarcoma

Journal: Revue medicale suisse
Published: October 03, 2024

Diagnostic features in paediatric MDS-EB with UBTF-internal tandem duplication: defining a unique subgroup.

Diagnostic features in paediatric MDS-EB with UBTF-internal tandem duplication: defining a unique subgroup.

Journal: Histopathology
Published: September 19, 2024

Prenatal Diagnosis of Warsaw Breakage Syndrome: Fetal Compound Heterozygous Variants in the DDX11 Gene Associated With Growth Restriction, Cerebral, and Extra-Cerebral Malformations.

Prenatal Diagnosis of Warsaw Breakage Syndrome: Fetal Compound Heterozygous Variants in the DDX11 Gene Associated With Growth Restriction, Cerebral, and Extra-Cerebral Malformations.

Journal: Prenatal diagnosis
Published: July 23, 2024

Development of MDS in Pediatric Patients with GATA2 Deficiency: Increased Histone Trimethylation and Deregulated Apoptosis as Potential Drivers of Transformation.

Development of MDS in Pediatric Patients with GATA2 Deficiency: Increased Histone Trimethylation and Deregulated Apoptosis as Potential Drivers of Transformation.

Journal: Cancers
Published: October 27, 2023

When the second comes first- rhabdomyosarcoma preceding heritable retinoblastoma- a case report.

When the second comes first- rhabdomyosarcoma preceding heritable retinoblastoma- a case report.

Journal: BMC ophthalmology
Published: May 22, 2023

Neuroblastic Tumors of the Adrenal Gland in Elderly Patients: A Case Report and Review of the Literature.

Neuroblastic Tumors of the Adrenal Gland in Elderly Patients: A Case Report and Review of the Literature.

Journal: Frontiers in pediatrics
Published: February 08, 2022
Showing 1-12 of 22

Last Updated: 09/26/2026