نتایج جستجو برای: bulbous plant

تعداد نتایج: 395562  

Journal: :Journal of medical genetics 1974
D D Weaver M M Cohen D W Smith

The tricho-rhino-phalan-geal syndrome is characterized by sparse fine hair, bulbous nose, and brachydac-tyly. The clinical and radiological findings of four affected family members, a father and his three children, are presented. Cardiovascular anomalies, previously unreported in this syndrome,were present in one of the children. Psychological and immunological evaluations were found to be esse...

1999
HONGRUI ZHANG LAURENCE A. MOUND YONGHUI XIE

A new genus and species, Yaobinthrips yangtzei, are described from Southwestern China sharing many character states with the Austro-Oriental genus Parabaliothrips within the Frankliniella genus-group. Within this group the new species is distinguished by the presence of tergal craspeda, a pair of uniquely bulbous modified setae on the fore tibiae, enlarged fore femora with a basal tooth, and pa...

Journal: :FEBS letters 2004
Ales Iglic Miha Fosnaric Henry Hägerstrand Veronika Kralj-Iglic

In this work, a hypothesis is presented that could explain the non-homogeneous lateral distribution of membrane components in Golgi vesicles. It is shown that the non-homogeneous lateral distribution of membrane components and the specific flattened shape of Golgi vesicles are strongly coupled. In agreement with experimental evidence, it is indicated that some of the membrane components may be ...

Journal: :journal of ornamental plants 2015
muhammad saleem iftikhar ahmad muhammad aslam khan

gladiolus (gladiolus grandiflorus l.), a popular bulbous cut flower, has high demand in both domestic (pakistani) as well as international markets. five potential, exotic cultivars of gladiolus, ‘cantate’, ‘corveira’, ‘eminence’, ‘essential’ and ‘fado’ were evaluated to determine the cultivar effects on yield and quality, to compare their relative performance and recommend their suitability for...

Journal: :Evidence-based Complementary and Alternative Medicine : eCAM 2007
Mayank Thakur V. K. Dixit

The bulbous roots of Dactylorhiza hatagirea (D.Don) Soo (Fam. Orchidacea) which are synonymous to the tubers of Orchis macula (Orchidaceae) and serve as source of Salep, are used traditionally in Indian subcontinent specially in the Northern region and Nepal as aphrodisiac and sexual stimulant. It is considered as a nutritive and restorative tonic and also as an alternative source of Salep used...

Journal: :American journal of medical genetics 2000
M A da Fonseca

Schimke immuno-osseous dysplasia is a rare autosomal recessive disorder that affects primarily bone, T lymphocytes, kidneys, and skin. The patients have a triangular face, broad nasal bridge, bulbous nose tip, small palpebral fissures, short neck, long upper lip, and low hairline. Dental abnormalities of affected patients have not been discussed in detail. The patient described in this clinical...

Journal: :Indian journal of pediatrics 1993
T Ishii

Tricho-rhino-phalangeal syndrome type I (TRPS I) is characterized by a bulbous nose, sparse hair and epiphyseal coning. Autosomal dominant and recessive transmission are suggested. The presence of cone-shaped epiphyses, the major complaint of patients due to swelling over the phalangeal joints, requires differential diagnosis among various syndromes. This paper, describing a ten-year-old girl w...

Journal: :AJNR. American journal of neuroradiology 2003
Gaurav Kumar Mauricio Castillo Craig A Buchman

A 31-year-old male patient presented with progressive mixed hearing loss since birth. A stapedectomy was attempted and was unsuccessful because of perilymph gushing. CT of the temporal bones showed bulbous dilatation of the fundi of the internal auditory canals and absence of the bone plates separating them from the base of the cochleas. This unusual abnormality was found after the attempted st...

2016
LAHARI SAIKIA

Rubinstein-Taybi syndrome is characterized by a broad thumb and bulbous hallux, short stature, intellectual disability and distinctive facial features [1]. It is a rare neuro-developmental disorder with a reported prevalence of 1 in 1,25,000 births [2]. Psychosis in RTS is highly infrequent with only a few scattered case reports [3]. A comprehensive literature search yielded only one case repor...

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