Suchergebnisse - "Clinical heterogeneity"

PubPharm (199)

1

22q11.2 Deletion Syndrome : Influence of Parental Origin on Clinical Heterogeneity

enthalten in: Genes | 2024

von de Wallau, M. | Xavier, A. | Moreno, C. | +11

2

Clinical profiles of adolescent personality pathology : a latent structure examination of the Semi-Structured Interview for Personality Functioning DSM-5 (STiP-5.1) in a help-seeking sample

enthalten in: Borderline personality disorder and emotion dysregulation | 2024

von Thomson, M. | Cavelti, M. | Lerch, S. | +5

3

Clinical profiles of adolescent personality pathology: a latent structure examination of the Semi-Structured Interview for Personality Functioning DSM-5 (STiP-5.1) in a help-seeking sample

enthalten in: Borderline Personality Disorder and Emotion Dysregulation | 2024

von Thomson, M. | Cavelti, M. | Lerch, S. | +5

4

An Effort to Identify Genetic Determinants in Siblings With Wilson Disease Manifesting Striking Clinical Heterogeneity : An Exome Profiling Study of Two Indian Families

enthalten in: Pediatric neurology | 2024

von Saha, A. | Das, S. | De, S. | +4

5

Two Cases of Sporadic Amyotrophic Lateral Sclerosis With Contrasting Clinical Phenotypes : Genetic Insights

enthalten in: Cureus | 2024

von Frolov, A. | Guzman, M. | Hayat, G. | +1

6

SYN1 variant causes X-linked neurodevelopmental disorders : a case report of variable clinical phenotypes in siblings

enthalten in: Frontiers in neurology | 2024

von Ren, B. | Wu, X. | Zhou, Y. | +2

7

Comparing the evidence for botulinum neurotoxin injections in paediatric anterior drooling : a scoping review

enthalten in: European journal of pediatrics | 2024

von Orriëns, L. | van Hulst, K. | van der Burg, J. | +3

8

An evolutionary perspective on complex neuropsychiatric disease

enthalten in: Neuron | 2024

von McClellan, J. | Zoghbi, A. | Buxbaum, J. | +17

9

Cross-Domain Identification of Multisite Major Depressive Disorder Using End-to-End Brain Dynamic Attention Network

in: IEEE Transactions on Neural Systems and Rehabilitation Engineering | 2024

von Xue Yuan | Maozhou Chen | Peng Ding | +6

10

SYN1 variant causes X-linked neurodevelopmental disorders: a case report of variable clinical phenotypes in siblings

in: Frontiers in Neurology | 2024

von Bin Ren | Xiaoyan Wu | Yuqiang Zhou | +2

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