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Visual Surveillance in Craniosynostoses.

• Authors : Nischal, Ken K.¹ .edu

• Source: American Orthoptic Journal. 2014, Vol. 64 Issue 1, p24-31. 8p.

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Apert syndrome in a newborn with premature fusion of skull bones, a rostral nose, and cleft palate: A case report.

• Authors : Faraji, Navid; Goli, Rasoul; Atharifar, Reza

Subjects: PREMATURE infants; CLEFT palate; GENETIC disorders

• Source: Clinical Case Reports; Aug2024, Vol. 12 Issue 8, p1-5, 5p

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Anesthesia for preoperative non-invasive intracranial pressure measurement in a child with Apert syndrome: a case report.

• Authors : Brandao Machado, Luciano; Madeira Brandao, Michele; Ferro, Andre

Subjects: INTRACRANIAL pressure; APERT syndrome; ANESTHESIA

• Source: Archives of Pediatric Neurosurgery; 2024, Vol. 6 Issue 1, p1-4, 4p

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Craniosynostosis: prenatal diagnosis by 2D/3D ultrasound, magnetic resonance imaging and computed tomography.

• Authors : Helfer, Talita Micheletti¹; Peixoto, Alberto Borges¹; Tonni, Gabriele¹

• Source: Medical Ultrasonography. Sep2016, Vol. 18 Issue 3, p378-385. 8p.

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Genetic Syndromes Associated with Craniosynostosis.

• Authors : Jung Min Ko¹

• Source: Journal of Korean Neurosurgical Society. May2016, Vol. 59 Issue 3, p187-191. 5p.

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CRANIOSYNOSTOSIS: ACROCEPHALOSYNDACTYLY (APERT SYNDROME) DIAGNOSED IN A NEWBORN.

• Authors : Stomnaroska, Orhideja¹ ; Danilovski, Dragan¹; Ivanovska, Sanja¹

• Source: Contributions / Prilozi (1857-9345). 2017, Vol. 38 Issue 3, p153-155. 3p.

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Apert Sendromu: Olgu Sunumu.

• Authors : Karaman, Ali¹ ; Kahveci, Hasan²

• Source: Medical Journal of Bakirkoy. Jun2013, Vol. 9 Issue 2, p81-84. 4p. 5 Black and White Photographs.

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Síndrome de Pfeiffer tipo 2. Informe de un caso y revisión de la literatura.

• Authors : Roldán-Arce, Jorge¹; Villarroel-Cortés, Camilo²

• Source: Acta Pediatrica de Mexico. ene/feb2013, Vol. 34 Issue 1, p43-47. 5p.

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Apert sendromu: Olgu Sunumu.

• Authors : Alanbay, İbrahim¹; Çoksüer, Hakan¹ ; Karaşahin, Emre¹

• Source: Perinatal Journal / Perinatoloji Dergisi. Apr2012, Vol. 20 Issue 1, p30-34. 5p. 2 Color Photographs, 1 Black and White Photograph.

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Germline mutation screening of the Saethre-Chotzen-associated genes TWIST1 and FGFR3 in families with BRCA1/2-negative breast cancer.

• Authors : Bergman, Annika¹; Sahlin, Pelle²; Emanuelsson, Monica³

• Source: Scandinavian Journal of Plastic & Reconstructive Surgery & Hand Surgery. Oct2009, Vol. 43 Issue 5, p251-255. 5p. 2 Charts, 1 Graph.

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