Results 141 to 150 of about 33,456 (303)

Lymphatic Abnormalities in Noonan Syndrome Extend Beyond Clinically Apparent Disease

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Lymphatic disease represents a well‐described manifestation of Noonan syndrome (NS), yet the full phenotypic spectrum remains incompletely characterized, especially in asymptomatic individuals. We conducted a cross‐sectional study including 10 individuals with NS (four with peripheral lymphedema and six without) and 10 age‐ and sex‐matched ...
Inger Norlyk Sheyanth   +7 more
wiley   +1 more source

Phenotype Expansion of Malan Syndrome: New Cases and a Review of the Literature

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Malan syndrome is an ultra‐rare overgrowth syndrome caused by pathogenic variants or deletions in nuclear factor one X (NFIX) located at 19p13.2. Here, we report a comprehensive literature review and phenotyping of known patients with Malan syndrome and present a novel cohort of eight patients.
Alex F. Nisbet   +10 more
wiley   +1 more source

Long‐Term Follow Up of Two Patients With Variants in the Cluster 1031‐1159 of TRRAP Gene: Expanding the Phenotype of Developmental Delay With or Without Dysmorphic Facies and Autism

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT The transformation/transcription domain‐associated protein (TRRAP) gene encodes a large multidomain protein, a member of the phosphatidylinositol 3‐kinase‐related kinase (PIKK) family. TRRAP is a component of the histone acetyltransferase (HAT) complex, and it plays an important role in gene transcription, DNA repair, and cell‐cycle regulation.
Roseli Maria Zechi‐Ceide   +10 more
wiley   +1 more source

The examination of anomalous world-experience in schizophrenia and other disorders: an exploratory investigation

open access: yes, 2013
There is extensive literature in the fields of psychiatry and clinical phenomenology documenting a set of sub-psychotic, sometimes subtle, subjective phenomena prominent in the phenomenology of schizophrenia-spectrum disorders.

core  

Response of an Infant With Presumed Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) to Ketone Supplementation

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Multiple Acyl‐CoA Dehydrogenase Deficiency (MADD) is an autosomal recessive inborn error of metabolism caused by biallelic pathogenic variants in one of three known genes: ETFA, ETFB, and ETFDH. It can cause multisystem dysfunction, including cardiomyopathy in severe cases.
Yutaka Furuta   +17 more
wiley   +1 more source

‘Sense of presence’ experiences in bereavement and their relationship to mental health: A critical examination of a continuing controversy

open access: yes, 2017
The experience of sensing the presence of the deceased is a common occurrence following bereavement. Although this experience tends to be reported as positive and meaningful by perceivers, for most of the twentieth century it has been described in ...
Steffen, E, Coyle, A
core  

Open Peer Comment to “Anomalous Cognition: An Umbrella Review of the Meta-Analytic Evidence”

open access: yesJournal of Anomalous Experience and Cognition, 2021
Stefan Schmidt
doaj   +1 more source

Phenomenology of Subjective Anomalous Experiences in People with Schizophrenia. [PDF]

open access: yesCult Med Psychiatry
Mondragón-Benítez O   +3 more
europepmc   +1 more source

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