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Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

Archives of Endocrinology and Metabolism, 2024-02, Vol.68, p.e220395

2024

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Perioperative management of tongue reduction surgery for macroglossia associated with Beckwith-Wiedemann syndrome -A retrospective evaluation of 14 patients--

Masui. The Japanese journal of anesthesiology, 2013-04, Vol.62 (4), p.416

2013

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Early presentation of right adrenal mass, hepatoblastoma and hepatic cavernous haemangioma in Beckwith-Wiedemann Syndrome

Medical journal of Malaysia, 2007-10, Vol.62 (4), p.345-346

2007

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Macroglossia and Beckwith-Wiedemann syndrome

Srpski arhiv za celokupno lekarstvo, 2011-05, Vol.139 (5-6), p.366-369

2011

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A case report of Beckwith-Wiedemann syndrome

Zhongguo dang dai er ke za zhi, 2010-05, Vol.12 (5), p.403

2010

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Beckwith-Wiedemann Syndrome (BWS): a case report and literature review

West African journal of medicine, 2003-01, Vol.22 (1), p.101-102

2003

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Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome: A new case and review of the literature

Cancer genetics and cytogenetics, 1992, Vol.58 (1), p.66-70

1992

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The Beckwith-Wiedemann syndrome. Seven new cases

American journal of diseases of children (1960), 1971-12, Vol.122 (6), p.515

1971

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The Beckwith-Wiedemann syndrome

American journal of diseases of children (1960), 1971-12, Vol.122 (6), p.520

1971

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Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome

Hormone research, 2000, Vol.54 (1), p.1-5

2000

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Wiedemann-Beckwith syndrome

Ergebnisse der inneren Medizin und Kinderheilkunde, 1993, Vol.61, p.303

1993

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Pancreatoblastoma

Journal of the Pancreas, 2007-01, Vol.8 (1), p.55-63

Saif, Muhammad Wasif

2007

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Epigenetic modification of the genetic material. Genomic imprinting and its significance for disease in human beings

Ugeskrift for læger, 2001-06, Vol.163 (23), p.3218

2001

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Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy

Annales de génétique, 1985, Vol.28 (2), p.93

1985

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A new case of Beckwith-Wiedemann syndrome with an 11p15 duplication of paternal origin [46,XY,-21,+der(21), t(11;21)(p15.2;q22.3)pat]

Acta geneticae medicae et gemellologiae, 1996, Vol.45 (1-2), p.245-250

1996

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Surgical correction of macroglossia in Beckwith-Wiedemann syndrome

Journal of oral surgery (1965), 1978-03, Vol.36 (3), p.212

1978

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Macroglossia in the Beckwith-Wiedemann syndrome

Transactions - American Academy of Ophthalmology and Otolaryngology (Section on Otolaryngology), 1977-01, Vol.84 (1), p.116

1977

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Beckwith-Wiedemann syndrome

Ryoikibetsu shokogun shirizu, 2001 (33), p.263

Okamoto, N

2001

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The Beckwith-Wiedemann syndrome

Srpski arhiv za celokupno lekarstvo, 1977-12, Vol.105 (12), p.1095

1977

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Propofol-fentanyl anesthesia for a 13-year-old patient with Beckwith-Wiedemann syndrome

Masui. The Japanese journal of anesthesiology, 2001-11, Vol.50 (11), p.1224

2001

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Anesthetic considerations in Beckwith-Wiedemann syndrome

Middle East journal of anaesthesiology, 1987-02, Vol.9 (1), p.127

1987

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Description of a case: Beckwith-Wiedemann syndrome

Minerva pediatrica, 1988-02, Vol.40 (2), p.113

1988

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Anesthetic management in a patient with Beckwith-Wiedemann syndrome

Masui. The Japanese journal of anesthesiology, 1994-09, Vol.43 (9), p.1389

1994

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A case of Beckwith-Wiedemann syndrome

Minerva pediatrica, 1988-12, Vol.40 (12), p.709

1988

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Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma

Cancer genetics and cytogenetics, 1986-10, Vol.23 (2), p.95-104

1986

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Beckwith-Wiedemann syndrome mimicking the classical form of congenital adrenal hyperplasia in newborn screening

Perioperative management of tongue reduction surgery for macroglossia associated with Beckwith-Wiedemann syndrome -A retrospective evaluation of 14 patients--

Early presentation of right adrenal mass, hepatoblastoma and hepatic cavernous haemangioma in Beckwith-Wiedemann Syndrome

Macroglossia and Beckwith-Wiedemann syndrome

A case report of Beckwith-Wiedemann syndrome

Beckwith-Wiedemann Syndrome (BWS): a case report and literature review

Paternal origin of 11p15 duplications in the Beckwith-Wiedemann syndrome: A new case and review of the literature

The Beckwith-Wiedemann syndrome. Seven new cases

The Beckwith-Wiedemann syndrome

Assessment of p57(KIP2) gene mutation in Beckwith-Wiedemann syndrome

Wiedemann-Beckwith syndrome

Pancreatoblastoma

Epigenetic modification of the genetic material. Genomic imprinting and its significance for disease in human beings

Beckwith-Wiedemann syndrome. Clinical comparison between patients with and without 11p15 trisomy

A new case of Beckwith-Wiedemann syndrome with an 11p15 duplication of paternal origin [46,XY,-21,+der(21), t(11;21)(p15.2;q22.3)pat]

Surgical correction of macroglossia in Beckwith-Wiedemann syndrome

Macroglossia in the Beckwith-Wiedemann syndrome

Beckwith-Wiedemann syndrome

The Beckwith-Wiedemann syndrome

Propofol-fentanyl anesthesia for a 13-year-old patient with Beckwith-Wiedemann syndrome

Anesthetic considerations in Beckwith-Wiedemann syndrome

Description of a case: Beckwith-Wiedemann syndrome

Anesthetic management in a patient with Beckwith-Wiedemann syndrome

A case of Beckwith-Wiedemann syndrome

Constitutional interstitial deletion of 11p11 and pericentric inversion of chromosome 9 in a patient with Wiedemann-Beckwith syndrome and hepatoblastoma

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