日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

How frequent is osteogenesis imperfecta in patients with idiopathic osteoporosis?: Case reports

特发性骨质疏松症患者中成骨不全的发生率有多高?:病例报告

Al Kaissi, Ali; Windpassinger, Christian; Chehida, Farid Ben; Ghachem, Maher Ben; Nassib, Nabil M; Kenis, Vladimir; Melchenko, Eugene; Morenko, Ekatrina; Ryabykh, Sergey; Hofstaetter, Jochen G; Grill, Franz; Ganger, Rudolf; Kircher, Susanne Gerit

The Diversity of the Clinical Phenotypes in Patients With Fibrodysplasia Ossificans Progressiva

进行性骨化性纤维发育不良患者的临床表型多样性

Al Kaissi, Ali; Kenis, Vladimir; Ben Ghachem, Maher; Hofstaetter, Jochen; Grill, Franz; Ganger, Rudolf; Kircher, Susanne Gerit

[Helicobacter pylori gastritis: assessment of OLGA and OLGIM staging systems]

[幽门螺杆菌胃炎:OLGA 和 OLGIM 分期系统的评估]

Ben Slama, Sana; Ben Ghachem, Dorra; Dhaoui, Amen; Jomni, Mohamed Taieb; Dougui, Mohamed Hédi; Bellil, Khadija

Dysmorphic facies and diffuse posterior spine ankylosis in a patient with unusual form of spondyloenchondrodysplasia (Spranger type IV)

患有罕见类型的脊椎软骨发育不良(Spranger IV 型)的患者出现面部畸形和弥漫性后脊柱强直

Al Kaissi, Ali; Ben Chehida, Farid; Ben Ghachem, Maher; Klaushofer, Klaus; Grill, Franz

Craniocervical junction malformation in a child with Oromandibular-limb hypogenesis-Möbius syndrome

患有口颌肢体发育不全-莫比乌斯综合征的儿童出现颅颈交界处畸形

Al Kaissi, Ali; Grill, Franz; Safi, Hatem; Ben Ghachem, Maher; Ben Chehida, Farid; Klaushofer, Klaus

Persistent torticollis, facial asymmetry, grooved tongue, and dolicho-odontoid process in connection with atlas malformation complex in three family subjects

三个家族成员均患有寰椎畸形复合征,并伴有持续性斜颈、面部不对称、舌沟和长齿状突。

Al Kaissi, Ali; Ben Chehida, Farid; Gharbi, Hassan; Ben Ghachem, Maher; Grill, Franz; Varga, Franz; Klaushofer, Klaus

Atlanto-axial rotatory fixation in a girl with Spondylocarpotarsal synostosis syndrome

一名患有脊椎腕跗骨融合综合征的女孩出现寰枢椎旋转固定

Al Kaissi, Ali; Ben Chehida, Farid; Gharbi, Hassan; Ben Ghachem, Maher; Grill, Franz; Klaushofer, Klaus

Subtotal amelia in a child with autosomal recessive hypohidrotic ectodermal dysplasia

患有常染色体隐性遗传性少汗型外胚层发育不良的儿童出现部分性无胚层

Al Kaissi, Ali; Ben Chehida, Farid; Nassib, Nabil; Safi, Hatem; Djnziri, Mrad; Ben Ghachem, Maher; Gharbi, Hassan