Results 171 to 180 of about 17,135 (242)

Unilateral craniosynostosis associated with ZIC1 gene mutation: a case report. [PDF]

J Surg Case Rep
Alsharef FK, Alraddadi KK, Aljared T.
europepmc   +1 more source

Deep phenotyping using foetal MRI. [PDF]

Med Genet
Kasprian G, Mitter C, Moser P.
europepmc   +1 more source

Prenatally diagnosed chromosome 1p36 deletions: a retrospective case series, literature review, and genotype-phenotype correlations. [PDF]

BMC Med Genomics
Liu N, Liu Z, Yi S, Li M, Cai H.
europepmc   +1 more source

Normal pressure hydrocephalus plus atypical presentation with symptomatic resolution following the restoration of CSF flow: illustrative case. [PDF]

J Neurosurg Case Lessons
Hatfield J, Carpenter K, Komisarow J, Friedman A, Morgenlander J.   +4 more
europepmc   +1 more source

Post feline infectious peritonitis progressive hydrocephalus: a case series. [PDF]

Front Vet Sci
Clouse M, Detwiler WR, Gibson EA, Eich J, Berg J, Joseph R.   +5 more
europepmc   +1 more source

Successful conservative management for ruptured basilar artery perforator aneurysm associated with early hematoma expansion in right temporal lobe without aneurysm rerupture: illustrative case. [PDF]

J Neurosurg Case Lessons
Nakajima H, Sato Y, Yago T, Tsuda K, Suzuki H.   +4 more
europepmc   +1 more source

Minilaparotomy-assisted approach for fetoscopic myelomeningocele closure. [PDF]

Neurosurg Focus Video
Holste K, Shainker S, Demehri F, Krispin E, Shamshirsaz A, Northam W.   +5 more
europepmc   +1 more source

Prenatally Diagnosed 7q11.23 Copy Number Variations: A Retrospective Case Series. [PDF]

Mol Genet Genomic Med
Yan J, Liu Z, Yi S, Liu N.
europepmc   +1 more source

Clinical and Molecular Spectrum of <i>PPP2R1A</i>-Related Neurodevelopmental Disorders: A Systematic Review. [PDF]

Genes (Basel)
Lee J, Ahn A, Yoo J, Lee S.
europepmc   +1 more source