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1
Neuroradiological findings in Alagille syndrome
Neuroradiological findings in Alagille syndrome
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Neuroradiological findings in Alagille syndrome

D'Amico, Alessandra ; Perillo, Teresa ; Cuocolo, Renato ; Ugga, Lorenzo ; Di Dato, Fabiola ; Caranci, Ferdinando ; Iorio, Raffaele

British journal of radiology, 2022-01, Vol.95 (1129), p.20201241-20201241 [Revista revisada por pares]

England: The British Institute of Radiology

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2
Cranial findings detected by second‐trimester ultrasound in fetuses with myelomeningocele: a systematic review
Cranial findings detected by second‐trimester ultrasound in fetuses with myelomeningocele: a systematic review
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Cranial findings detected by second‐trimester ultrasound in fetuses with myelomeningocele: a systematic review

Kunpalin, Y ; Richter, J ; Mufti, N ; Bosteels, J ; Ourselin, S ; De Coppi, P ; Thompson, D ; David, AL ; Deprest, J

BJOG : an international journal of obstetrics and gynaecology, 2021-01, Vol.128 (2), p.366-374 [Revista revisada por pares]

England: Wiley Subscription Services, Inc

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3
Three‐dimensional ultrasound imaging of the fetal skull and face
Three‐dimensional ultrasound imaging of the fetal skull and face
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Three‐dimensional ultrasound imaging of the fetal skull and face

Tutschek, B. ; Blaas, H.‐G. K. ; Abramowicz, J. ; Baba, K. ; Deng, J. ; Lee, W. ; Merz, E. ; Platt, L. ; Pretorius, D. ; Timor‐Tritsch, I. E. ; Gindes, L.

Ultrasound in obstetrics & gynecology, 2017-07, Vol.50 (1), p.7-16 [Revista revisada por pares]

Chichester, UK: John Wiley & Sons, Ltd

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4
The Relationship between Brachycephalic Head Features in Modern Persian Cats and Dysmorphologies of the Skull and Internal Hydrocephalus
The Relationship between Brachycephalic Head Features in Modern Persian Cats and Dysmorphologies of the Skull and Internal Hydrocephalus
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The Relationship between Brachycephalic Head Features in Modern Persian Cats and Dysmorphologies of the Skull and Internal Hydrocephalus

Schmidt, M.J. ; Kampschulte, M. ; Enderlein, S. ; Gorgas, D. ; Lang, J. ; Ludewig, E. ; Fischer, A. ; Meyer‐Lindenberg, A. ; Schaubmar, A.R. ; Failing, K. ; Ondreka, N.

Journal of veterinary internal medicine, 2017-09, Vol.31 (5), p.1487-1501 [Revista revisada por pares]

United States: John Wiley and Sons Inc

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5
A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly
A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly
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A targeted sequencing panel identifies rare damaging variants in multiple genes in the cranial neural tube defect, anencephaly

Ishida, M. ; Cullup, T. ; Boustred, C. ; James, C. ; Docker, J. ; English, C. ; Lench, N. ; Copp, A.J. ; Moore, G.E. ; Greene, N.D.E. ; Stanier, P.

Clinical genetics, 2018-04, Vol.93 (4), p.870-879 [Revista revisada por pares]

Oxford, UK: Blackwell Publishing Ltd

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6
Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members
Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members
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Cortical dysplasia resembling human type 2 lissencephaly in mice lacking all three APP family members

Herms, Jochen ; Anliker, Brigitte ; Heber, Sabine ; Ring, Sabine ; Fuhrmann, Martin ; Kretzschmar, Hans ; Sisodia, Sangram ; Müller, Ulrike

The EMBO journal, 2004-10, Vol.23 (20), p.4106-4115 [Revista revisada por pares]

Chichester, UK: John Wiley & Sons, Ltd

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7
Gpr177/mouse Wntless is essential for Wnt‐mediated craniofacial and brain development
Gpr177/mouse Wntless is essential for Wnt‐mediated craniofacial and brain development
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Gpr177/mouse Wntless is essential for Wnt‐mediated craniofacial and brain development

Fu, Jiang ; Ivy Yu, Hsiao‐Man ; Maruyama, Takamitsu ; Mirando, Anthony J. ; Hsu, Wei

Developmental dynamics, 2011-02, Vol.240 (2), p.365-371 [Revista revisada por pares]

New York: Wiley‐Liss, Inc

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8
Nell‐1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2+/− mice
Nell‐1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2+/− mice
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Nell‐1, a key functional mediator of Runx2, partially rescues calvarial defects in Runx2+/− mice

Zhang, Xinli ; Ting, Kang ; Bessette, Catherine M ; Culiat, Cymbeline T ; Sung, Sang Jin ; Lee, Haofu ; Chen, Feng ; Shen, Jia ; Wang, James J ; Kuroda, Shun'ichi ; Soo, Chia

Journal of bone and mineral research, 2011-04, Vol.26 (4), p.777-791 [Revista revisada por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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9
Cranial base abnormalities in osteogenesis imperfecta: Phenotypic and genotypic determinants
Cranial base abnormalities in osteogenesis imperfecta: Phenotypic and genotypic determinants
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Cranial base abnormalities in osteogenesis imperfecta: Phenotypic and genotypic determinants

Cheung, Moira S ; Arponen, Heidi ; Roughley, Peter ; Azouz, Michel E ; Glorieux, Francis H ; Waltimo‐Sirén, Janna ; Rauch, Frank

Journal of bone and mineral research, 2011-02, Vol.26 (2), p.405-413 [Revista revisada por pares]

Hoboken: Wiley Subscription Services, Inc., A Wiley Company

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10
Risk of ultrasound‐detected neonatal brain abnormalities in intrauterine growth‐restricted fetuses born between 28 and 34 weeks' gestation: relationship with gestational age at birth and fetal Doppler parameters
Risk of ultrasound‐detected neonatal brain abnormalities in intrauterine growth‐restricted fetuses born between 28 and 34 weeks' gestation: relationship with gestational age at birth and fetal Doppler parameters
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Risk of ultrasound‐detected neonatal brain abnormalities in intrauterine growth‐restricted fetuses born between 28 and 34 weeks' gestation: relationship with gestational age at birth and fetal Doppler parameters

Cruz‐Martinez, R. ; Tenorio, V. ; Padilla, N. ; Crispi, F. ; Figueras, F. ; Gratacos, E.

Ultrasound in obstetrics & gynecology, 2015-10, Vol.46 (4), p.452-459 [Revista revisada por pares]

Chichester, UK: John Wiley & Sons, Ltd

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