Scalp-Ear-Nipple Syndrome Latest Advances

Find the Latest Research About Scalp-Ear-Nipple Syndrome

Last Updated: 04/28/2026

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Found 12 publications

Preoperative computed tomography-guided transscapular sens-cure needle localization for pulmonary nodule located behind the scapula.

Preoperative computed tomography-guided transscapular sens-cure needle localization for pulmonary nodule located behind the scapula.

Journal: Journal of cardiothoracic surgery
Published: September 22, 2022

Point Shear Wave Elastography by ElastPQ for Fibrosis Screening in Patients with NAFLD: A Prospective, Multicenter Comparison to Vibration-Controlled Elastography.

Point Shear Wave Elastography by ElastPQ for Fibrosis Screening in Patients with NAFLD: A Prospective, Multicenter Comparison to Vibration-Controlled Elastography.

Journal: Ultraschall in der Medizin (Stuttgart, Germany : 1980)
Published: February 28, 2022

Scalp-Ear-Nipple syndrome: first report of a Potassium channel tetramerization domain-containing 1 in-frame insertion and review of the literature.

Scalp-Ear-Nipple syndrome: first report of a Potassium channel tetramerization domain-containing 1 in-frame insertion and review of the literature.

Journal: Clinical dysmorphology
Published: August 30, 2021

Breast reconstruction via fat grafting for a patient with bilateral congenital amastia (Finlay-Marks syndrome).

Breast reconstruction via fat grafting for a patient with bilateral congenital amastia (Finlay-Marks syndrome).

Journal: Congenital anomalies
Published: November 27, 2020

KCTD1 mutants in scalp‑ear‑nipple syndrome and AP‑2α P59A in Char syndrome reciprocally abrogate their interactions, but can regulate Wnt/β‑catenin signaling.

KCTD1 mutants in scalp‑ear‑nipple syndrome and AP‑2α P59A in Char syndrome reciprocally abrogate their interactions, but can regulate Wnt/β‑catenin signaling.

Journal: Molecular medicine reports
Published: June 19, 2019

Molecular basis of the scalp-ear-nipple syndrome unraveled by the characterization of disease-causing KCTD1 mutants.

Molecular basis of the scalp-ear-nipple syndrome unraveled by the characterization of disease-causing KCTD1 mutants.

Journal: Scientific reports
Published: April 18, 2019

Mutations in KCTD1 cause scalp-ear-nipple syndrome.

Mutations in KCTD1 cause scalp-ear-nipple syndrome.

Journal: American journal of human genetics
Published: January 30, 2013

Finlay-Marks syndrome: report of two siblings and review of literature.

Finlay-Marks syndrome: report of two siblings and review of literature.

Journal: American journal of medical genetics. Part A
Published: June 26, 2011

Infantile cirrhosis of the liver (Sen's syndrome).

Infantile cirrhosis of the liver (Sen's syndrome).

Journal: Annales paediatrici. International review of pediatrics
Published: January 01, 1962

Infantile cirrhosis of the liver (Sen's syndrome) with particular reference to the sulphur-containing amino acids.

Infantile cirrhosis of the liver (Sen's syndrome) with particular reference to the sulphur-containing amino acids.

Journal: The Journal of pediatrics
Published: August 01, 1960

A contribution to our knowledge of Myrsidea (Mallophaga: Amblycera) occurring on Turdidae (sens. lat.).

A contribution to our knowledge of Myrsidea (Mallophaga: Amblycera) occurring on Turdidae (sens. lat.).

Journal: Pakistan journal of health
Published: January 01, 1956

The Waterhouse-Friderich sen syndrome; a case report.

The Waterhouse-Friderich sen syndrome; a case report.

Journal: Manitoba medical review
Published: May 01, 1947
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Last Updated: 04/28/2026