標(biāo)題: Titlebook: Bone Dysplasias of Infancy; A Radiological Atlas Bryan J. Cremin,Peter Beighton Book 1978 Springer-Verlag Berlin Heidelberg 1978 Bone.Dyspl [打印本頁] 作者: Radiofrequency 時(shí)間: 2025-3-21 19:19
書目名稱Bone Dysplasias of Infancy影響因子(影響力)
書目名稱Bone Dysplasias of Infancy影響因子(影響力)學(xué)科排名
書目名稱Bone Dysplasias of Infancy網(wǎng)絡(luò)公開度
書目名稱Bone Dysplasias of Infancy網(wǎng)絡(luò)公開度學(xué)科排名
書目名稱Bone Dysplasias of Infancy被引頻次
書目名稱Bone Dysplasias of Infancy被引頻次學(xué)科排名
書目名稱Bone Dysplasias of Infancy年度引用
書目名稱Bone Dysplasias of Infancy年度引用學(xué)科排名
書目名稱Bone Dysplasias of Infancy讀者反饋
書目名稱Bone Dysplasias of Infancy讀者反饋學(xué)科排名
作者: inflame 時(shí)間: 2025-3-21 23:52 作者: 假 時(shí)間: 2025-3-22 00:38 作者: 天文臺(tái) 時(shí)間: 2025-3-22 05:47
https://doi.org/10.1007/978-3-662-12322-5eviewed these conditions and defined the Saldino-Noonan and Majewski forms while . et al. (1977) reported a third variety. There is some overlap in these descriptions and delineation is not yet complete.作者: 可能性 時(shí)間: 2025-3-22 10:23
Siegfried B?hme,Walter Fricke,Gert Zechhe term “nanisme diastrophique”, which was used by these authors, refers to the twisted habitus in this serious disorder. Diastrophic dysplasia is not uncommon and . et al. (1972) were able to assemble a series of 51 cases.作者: enumaerate 時(shí)間: 2025-3-22 15:57
Astronomy and Astrophysics Abstractsl malalignment and shortening of the trunk relative to the limbs. Case reports can be recognized in the early literature under the redundant title “hyperplastic achondroplasia”. There are different varieties of this condition, including a rare, severe form which is lethal in the neonate.作者: Suppository 時(shí)間: 2025-3-22 20:41 作者: 符合規(guī)定 時(shí)間: 2025-3-22 22:16 作者: LOPE 時(shí)間: 2025-3-23 02:40 作者: asthma 時(shí)間: 2025-3-23 08:32 作者: 富饒 時(shí)間: 2025-3-23 13:29 作者: flamboyant 時(shí)間: 2025-3-23 14:22 作者: Wernickes-area 時(shí)間: 2025-3-23 18:50
Positional Astronomy, Celestial Mechanics,nlethal form of short-limbed dwarfism. The eponym “Grebe syndrome” is now applied to this entity, while “achondrogenesis” pertains to the lethal condition which forms the subject of this chapter. The nosological situation has been further confused by the recognition of subtypes of achondrogenesis an作者: 小爭(zhēng)吵 時(shí)間: 2025-3-23 22:22
https://doi.org/10.1007/978-3-662-12322-5eviewed these conditions and defined the Saldino-Noonan and Majewski forms while . et al. (1977) reported a third variety. There is some overlap in these descriptions and delineation is not yet complete.作者: cluster 時(shí)間: 2025-3-24 04:00
https://doi.org/10.1007/978-3-662-12322-5 and dysplasia epiphysealis punctata. The disorder is now conventionally subdivided into the potentially lethal rhizomelic autosomal recessive type and the more benign, autosomal dominant Conradi-Hünermann form (. et al., 1971). An X-linked dominant variety of the latter has recently been reported a作者: Synovial-Fluid 時(shí)間: 2025-3-24 10:24
Siegfried B?hme,Walter Fricke,Gert Zechhe term “nanisme diastrophique”, which was used by these authors, refers to the twisted habitus in this serious disorder. Diastrophic dysplasia is not uncommon and . et al. (1972) were able to assemble a series of 51 cases.作者: 起草 時(shí)間: 2025-3-24 11:25
Astronomy and Astrophysics Abstractsl malalignment and shortening of the trunk relative to the limbs. Case reports can be recognized in the early literature under the redundant title “hyperplastic achondroplasia”. There are different varieties of this condition, including a rare, severe form which is lethal in the neonate.作者: 休息 時(shí)間: 2025-3-24 16:47 作者: 領(lǐng)袖氣質(zhì) 時(shí)間: 2025-3-24 20:51 作者: 嚴(yán)峻考驗(yàn) 時(shí)間: 2025-3-25 02:49 作者: 原來 時(shí)間: 2025-3-25 05:24
Astronomical Instruments and Techniques,re the marked changes are present at birth, and the tarda variety, in which bone fragility only becomes evident in later childhood. The eponyms “Vrolik” and “Porak-Durante” are sometimes applied to the former type, and “Lobstein” and “Van de Hoeve” to the latter. It must be emphasized that although 作者: Climate 時(shí)間: 2025-3-25 10:36 作者: 愛國(guó)者 時(shí)間: 2025-3-25 14:05
Clinical and Genetic Evaluation of the Neonate with Skeletal Dysplasia,on the accumulation and correlation of information from a number of sources and as several of the skeletal dysplasias are potentially lethal the opportunity to obtain objective evidence may be fleeting. In these circumstances, a full clinical, genetic, and radiographic evaluation is imperative.作者: Glower 時(shí)間: 2025-3-25 18:53
Lethal Short Rib-Polydactyly Syndromes,eviewed these conditions and defined the Saldino-Noonan and Majewski forms while . et al. (1977) reported a third variety. There is some overlap in these descriptions and delineation is not yet complete.作者: Perennial長(zhǎng)期的 時(shí)間: 2025-3-25 23:13 作者: 暖昧關(guān)系 時(shí)間: 2025-3-26 03:52 作者: Crater 時(shí)間: 2025-3-26 06:04 作者: 水土 時(shí)間: 2025-3-26 10:40 作者: 良心 時(shí)間: 2025-3-26 15:52 作者: 心胸狹窄 時(shí)間: 2025-3-26 19:10 作者: 性學(xué)院 時(shí)間: 2025-3-26 22:01
https://doi.org/10.1007/978-3-662-12313-3Thanatophoric dysplasia was differentiated from achondroplasia by . et al. (1967). The name is derived from the Greek term for death-bearing. This disorder, which has well-defined radiographic features, is the commonest form of fatal neonatal dwarfism.作者: Interregnum 時(shí)間: 2025-3-27 04:32
Periodicals, Proceedings, Books, Activities,This condition, described in a pair of siblings by . et al. (1955), is also known as infantile thoracic dystrophy, thoracopelvicphalangeal dystrophy, and the Jeune syndrome. The stigmata and clinical course are very variable and it is possible that the disorder is heterogeneous (. and ., 1974; . and ., 1976).作者: 猜忌 時(shí)間: 2025-3-27 05:21
https://doi.org/10.1007/978-3-662-12316-4. and . (1940) delineated this syndrome, of which more than 120 cases have now been reported. A large proportion of these have occurred in a consanguineous community, the Amish of Pennsylvania, USA (. et al., 1964; . and ., 1969).作者: champaign 時(shí)間: 2025-3-27 12:28 作者: PANT 時(shí)間: 2025-3-27 16:54 作者: Albinism 時(shí)間: 2025-3-27 21:21
Astronomical Instruments and Techniques,Cleidocranial dysplasia is a benign condition in which varying degrees of clavicular maldevelopment are associated with characteristic changes in the skull. The disorder is unlikely to be suspected in a neonate unless a positive family history has prompted radiographic studies.作者: Halfhearted 時(shí)間: 2025-3-28 01:04 作者: 濃縮 時(shí)間: 2025-3-28 04:11
Asphyxiating Thoracic Dysplasia,This condition, described in a pair of siblings by . et al. (1955), is also known as infantile thoracic dystrophy, thoracopelvicphalangeal dystrophy, and the Jeune syndrome. The stigmata and clinical course are very variable and it is possible that the disorder is heterogeneous (. and ., 1974; . and ., 1976).作者: 尾巴 時(shí)間: 2025-3-28 08:13 作者: MAL 時(shí)間: 2025-3-28 12:36 作者: CHARM 時(shí)間: 2025-3-28 15:07
Achondroplasia,Achondroplasia is by far the most common form of disproportionate dwarfism. Until recently the majority of newborn short-limbed dwarfs have been misdiagnosed as achondroplasts or achondroplasia variants and this has been the source of considerable confusion, both in the literature and in clinical practice (. and ., 1971).作者: JIBE 時(shí)間: 2025-3-28 18:54
Cleido-Cranial Dysplasia,Cleidocranial dysplasia is a benign condition in which varying degrees of clavicular maldevelopment are associated with characteristic changes in the skull. The disorder is unlikely to be suspected in a neonate unless a positive family history has prompted radiographic studies.作者: bifurcate 時(shí)間: 2025-3-29 00:21 作者: 變形 時(shí)間: 2025-3-29 05:33
https://doi.org/10.1007/978-3-662-12322-5o a feature of many other unrelated disorders, including:.In all these conditions, as well as in the conventional forms of chondrodysplasia punctata, the stippling in the survivors disappears by the end of the second year of life.作者: Inkling 時(shí)間: 2025-3-29 08:14 作者: Tortuous 時(shí)間: 2025-3-29 14:40
has demanded such a degree of specialisation that no single individual can be conversant with all the information available. More and more emphasis, therefore, has been placed on the importance of teamwork and close collaboration between associated disciplines. The bone dysplasias of infancy repres作者: 證實(shí) 時(shí)間: 2025-3-29 18:28 作者: harpsichord 時(shí)間: 2025-3-29 22:25
Positional Astronomy, Celestial Mechanics,tion which forms the subject of this chapter. The nosological situation has been further confused by the recognition of subtypes of achondrogenesis and by the application of overlapping numeric designations.作者: 褻瀆 時(shí)間: 2025-3-30 00:47 作者: 厚臉皮 時(shí)間: 2025-3-30 04:24
Positional Astronomy, Celestial Mechanics,congenita, tarda, and latent varieties. This separation may be artificial as . et al. (1972) have identified mild and severe forms within the same kindred. Nevertheless, the congenita form is often lethal and hypophosphatasia warrants consideration in this context.作者: Rinne-Test 時(shí)間: 2025-3-30 09:01 作者: –DOX 時(shí)間: 2025-3-30 16:01 作者: Immunoglobulin 時(shí)間: 2025-3-30 19:30 作者: Guileless 時(shí)間: 2025-3-30 21:26
Hypophosphatasia,congenita, tarda, and latent varieties. This separation may be artificial as . et al. (1972) have identified mild and severe forms within the same kindred. Nevertheless, the congenita form is often lethal and hypophosphatasia warrants consideration in this context.作者: MOAT 時(shí)間: 2025-3-31 00:51 作者: 誘拐 時(shí)間: 2025-3-31 06:17 作者: 挑剔小責(zé) 時(shí)間: 2025-3-31 11:09
Book 1978e affected child in many instances, but, almost of greater value, genetic counselling concerning the chance of subsequent offspring being similarly affected has become available to parents. Most radiologists have little opportunity of becoming familiar with this rapidly widening field of diagnosis, 作者: 槍支 時(shí)間: 2025-3-31 16:27 作者: 平常 時(shí)間: 2025-3-31 21:12 作者: 傲慢物 時(shí)間: 2025-4-1 01:39 作者: 草本植物 時(shí)間: 2025-4-1 04:43
Radiographic Techniques,sing fetal maturity and position. When there is the possibility of skeletal dysplasia, however, radiography is superior to all other methods in the third trimester. The authors do not associate themselves with the indiscriminate use of radiography and recognize that this is an emotive subject. Never作者: 半身雕像 時(shí)間: 2025-4-1 06:25 作者: inflate 時(shí)間: 2025-4-1 14:13
Lethal Short Rib-Polydactyly Syndromes,eviewed these conditions and defined the Saldino-Noonan and Majewski forms while . et al. (1977) reported a third variety. There is some overlap in these descriptions and delineation is not yet complete.作者: macabre 時(shí)間: 2025-4-1 16:47
Chondrodysplasia Punctata, and dysplasia epiphysealis punctata. The disorder is now conventionally subdivided into the potentially lethal rhizomelic autosomal recessive type and the more benign, autosomal dominant Conradi-Hünermann form (. et al., 1971). An X-linked dominant variety of the latter has recently been reported a作者: FOR 時(shí)間: 2025-4-1 21:17
