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The Journal of Pain
|
January 11, 2024
Reduced Gray Matter Volume and Cortical Thickness in Patients With Small-Fiber Neuropathy
Sebastian Scheliga, Maike F Dohrn, Ute Habel, et al.
Pain
|
May 23, 2025
Microneurographic portrait of 19 patients with small fiber neuropathy: a pilot study
Andrea Beisswanger, Greta Z Peschke, Noortje W M V D Braak, et al.
European Journal of Pain (London, England)
|
August 28, 2024
Painful stimulation increases functional connectivity between supplementary motor area and thalamus in patients with small fibre neuropathy
Sebastian Scheliga, Maike F Dohrn, Thilo Kellermann, et al.
The Journal of Pain
|
June 26, 2025
Reduced functional resting-state connectivity in chronic pain patients with small fiber neuropathy
Sebastian Scheliga, Han-Gue Jo, Maike F Dohrn, et al.
Clinical Genetics
|
December 12, 2024
Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study
Luise Kessler, Jeremias Krause, Florian Kraft, et al.
Cancers
|
July 20, 2021
Single Cell Genetic Profiling of Tumors of Breast Cancer Patients Aged 50 Years and Older Reveals Enormous Intratumor Heterogeneity Independent of Individual Prognosis
Anna-Sophie Liegmann, Kerstin Heselmeyer-Haddad, Annette Lischka, et al.
Neuropediatrics
|
April 28, 2025
Genetic Variants and Clinical Phenotyping in 39 Pediatric Patients with Neuropathic Pain
Annegret Quade, Annette Lischka, Simone Albani, et al.
The American Journal of Pathology
|
May 17, 2020
High Levels of Chromosomal Copy Number Alterations and TP53 Mutations Correlate with Poor Outcome in Younger Breast Cancer Patients
Ayla Koçak, Kerstin Heselmeyer-Haddad, Annette Lischka, et al.
The Journal of General Physiology
|
October 24, 2025
Altered NaV1.9 channel activity in two Tyr66Ser variant carriers with small fiber dysfunction
Noortje W M van den Braak, Samuel Kuehs, Greta Z Peschke, et al.
Deutsches Arzteblatt International
|
March 19, 2026
Exome and Genome Sequencing for the Diagnosis of Rare Diseases
Miriam Elbracht, Jeremias Krause, Larissa Mattern, et al.
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of 3
Search research articles
Search
Showing results (11-20 of 23) with videos related to
Sort By:
Page
of 3
The Journal of Pain
|
January 11, 2024
Reduced Gray Matter Volume and Cortical Thickness in Patients With Small-Fiber Neuropathy
Sebastian Scheliga, Maike F Dohrn, Ute Habel, et al.
Pain
|
May 23, 2025
Microneurographic portrait of 19 patients with small fiber neuropathy: a pilot study
Andrea Beisswanger, Greta Z Peschke, Noortje W M V D Braak, et al.
European Journal of Pain (London, England)
|
August 28, 2024
Painful stimulation increases functional connectivity between supplementary motor area and thalamus in patients with small fibre neuropathy
Sebastian Scheliga, Maike F Dohrn, Thilo Kellermann, et al.
The Journal of Pain
|
June 26, 2025
Reduced functional resting-state connectivity in chronic pain patients with small fiber neuropathy
Sebastian Scheliga, Han-Gue Jo, Maike F Dohrn, et al.
Clinical Genetics
|
December 12, 2024
Diagnostic Use of Genome Sequencing in Patients With 11p15.5 Imprinting Disorder Features: A Pilot Study
Luise Kessler, Jeremias Krause, Florian Kraft, et al.
Cancers
|
July 20, 2021
Single Cell Genetic Profiling of Tumors of Breast Cancer Patients Aged 50 Years and Older Reveals Enormous Intratumor Heterogeneity Independent of Individual Prognosis
Anna-Sophie Liegmann, Kerstin Heselmeyer-Haddad, Annette Lischka, et al.
Neuropediatrics
|
April 28, 2025
Genetic Variants and Clinical Phenotyping in 39 Pediatric Patients with Neuropathic Pain
Annegret Quade, Annette Lischka, Simone Albani, et al.
The American Journal of Pathology
|
May 17, 2020
High Levels of Chromosomal Copy Number Alterations and TP53 Mutations Correlate with Poor Outcome in Younger Breast Cancer Patients
Ayla Koçak, Kerstin Heselmeyer-Haddad, Annette Lischka, et al.
The Journal of General Physiology
|
October 24, 2025
Altered NaV1.9 channel activity in two Tyr66Ser variant carriers with small fiber dysfunction
Noortje W M van den Braak, Samuel Kuehs, Greta Z Peschke, et al.
Deutsches Arzteblatt International
|
March 19, 2026
Exome and Genome Sequencing for the Diagnosis of Rare Diseases
Miriam Elbracht, Jeremias Krause, Larissa Mattern, et al.
Page
of 3