نتایج جستجو برای: schinzel equation

تعداد نتایج: 229987  

Journal: :Computers & Mathematics with Applications 2010

Journal: :Revista do Hospital das Clinicas 2004
Lilian Maria José Albano Paula Priscila Ohara Sakae Marta Maria Galli Bozzo Mataloun Clea Rodrigues Leone Débora R Bertola Chong Ae Kim

Schinzel-Giedion syndrome is a rare autosomal recessive disorder characterized by coarse facies, midface retraction, hypertrichosis, multiple skeletal anomalies, and cardiac and renal malformations. Craniofacial abnormalities of this syndrome sometimes resemble a storage or metabolic disease. The pathogenesis of the disease remains unknown. The objective of this report was to emphasize the impo...

2011
Elizabeth McPherson

Other names: Schinzel-Giedion syndrome. Note: The use of the long form of the name, SchinzelGiedion midface retraction syndrome, is preferred to prevent confusion with Schinzel ulnar-mammary syndrome, a completely unrelated and clinically nonoverlapping condition also described by Dr Schinzel. Inheritance: Schinzel-Giedion midface retraction syndrome is presumed to be inherited as autosomal rec...

2011
Elizabeth McPherson

Other names: Schinzel-Giedion syndrome. Note: The use of the long form of the name, SchinzelGiedion midface retraction syndrome, is preferred to prevent confusion with Schinzel ulnar-mammary syndrome, a completely unrelated and clinically nonoverlapping condition also described by Dr Schinzel. Inheritance: Schinzel-Giedion midface retraction syndrome is presumed to be inherited as autosomal rec...

2017
Nozomi Hishimura Michiko Watari Hiroki Ohata Naho Fuseya Sadae Wakiguchi Tomoharu Tokutomi Kouji Okuhara Nobuhiro Takahashi Susumu Iizuka Hiroshi Yamamoto Takashi Mishima Satoko Fujieda Ryoji Kobayashi Kazutoshi Cho Yukiko Kuroda Kenji Kurosawa Hidefumi Tonoki

We report two Japanese patients with Schinzel-Giedion syndrome. When polyhydramnios is observed, additional fetal findings such as overlapping fingers, hydrocephalus, hydronephrosis, and very characteristic facial appearance comprising high, prominent forehead, hypertelorism, and depressed nasal root may suggest Schinzel-Giedion syndrome.

Journal: :American journal of medical genetics. Part A 2015
Ellaine Carvalho Rachel Honjo Monize Magalhães Guilherme Yamamoto Katia Rocha Michel Naslavsky Mayana Zatz Maria Rita Passos-Bueno Chong Kim Debora Bertola

Schinzel-Giedion syndrome is a rare autosomal dominant disorder comprising postnatal growth failure, profound developmental delay, seizures, facial dysmorphisms, genitourinary, skeletal, neurological, and cardiac defects. It was recently revealed that Schinzel-Giedion syndrome is caused by de novo mutations in SETBP1, but there are few reports of this syndrome with molecular confirmation. We de...

1992
Martin Klazar

We survey in detail extremal results on Davenport–Schinzel sequences and their generalizations, from the seminal papers of H. Davenport and A. Schinzel in 1965 to present. We discuss geometric and enumerative applications, generalizations to colored trees, and generalizations to hypergraphs. Eleven illustrative examples with proofs are given and nineteen open problems are posed.

2012
K. H. F. CHENG H. C. WILLIAMS Alf van der Poorten

It is well known that the regular continued fraction expansion of a quadratic irrational is symmetric about its centre; we refer to this symmetry as horizontal. However, an additional vertical symmetry is exhibited by the continued fraction expansions arising from a family of quadratics known as Schinzel sleepers. This paper provides a method for generating every Schinzel sleeper and investigat...

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