نتایج جستجو برای: caudal regression syndrome

تعداد نتایج: 930161  

Journal: :Mechanisms of Development 1997
Karen Marom Eli Shapira Abraham Fainsod

The caudal genes in vertebrates as in invertebrates assume a posterior position along the anterior-posterior axis and they appear to regulate the expression of the Hox genes. The third chicken caudal gene, Cdx-C, was cloned. Extensive comparisons of the sequence of this protein to the other known members of this homeobox family has lead to the suggestion that vertebrate genomes contain three me...

Journal: :Journal of Pediatric Surgery Case Reports 2013

2015
Solmaz Abdolrahimzadeh Valeria Fameli Roberto Mollo Maria Teresa Contestabile Andrea Perdicchi Santi Maria Recupero

Noteworthy heterogeneity exists in the rare diseases associated with childhood glaucoma. Primary congenital glaucoma is mostly sporadic; however, 10% to 40% of cases are familial. CYP1B1 gene mutations seem to account for 87% of familial cases and 27% of sporadic cases. Childhood glaucoma is classified in primary and secondary congenital glaucoma, further divided as glaucoma arising in dysgenes...

Journal: :Sexual development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation 2007
U Drews

The development of a vagina as a separate outlet of the birth canal evolves at the transition of egg laying species to eutherian mammals. The derivation of the vagina from the Wolffian and Müllerian ducts and the contribution of the urogenital sinus are still open questions. Here experiments with the complete androgen receptor defect in the testicular feminisation (Tfm) mouse are reported which...

Journal: :Neurology 2018
Raffaele Iorio

Gasperini syndrome is a rare crossed brainstem syndrome characterized by ipsilateral impairment of the VI, VII, and occasionally VIII cranial nerves and contralateral sensory loss. The syndrome, initially described by Ubaldo Gasperini in 1912, results from a lesion of the caudal pons tegmentum (figure e-1, links.lww.com/WNL/A47). The most frequent cause is the occlusion of the long circumferent...

Journal: :The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques 1980
C R Bamford M S Smith W A Sibley

From the Department of Neurology, Arizona Health Sciences Center, University of Arizona. It seems remarkable that multiple sclerosis does not commonly cause a Horner's syndrome for this syndrome is a manifestation of many different disease processes which affect the caudal brainstem and cervical spinal cord, as does multiple sclerosis. Yet, a careful review of the literature detailing the clini...

2017
Ruth Diez del Corral Aixa V. Morales

During vertebrate embryonic development, the spinal cord is formed by the neural derivatives of a neuromesodermal population that is specified at early stages of development and which develops in concert with the caudal regression of the primitive streak. Several processes related to spinal cord specification and maturation are coupled to this caudal extension including neurogenesis, ventral pa...

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