Al Kaissi A[au] - Search Results

Year	Number of Results
1983	1
2003	2
2004	1
2005	4
2006	4
2007	8
2008	17
2009	9
2010	5
2011	7
2012	6
2013	11
2014	10
2015	4
2016	5
2017	7
2018	3
2019	5
2020	6
2021	4
2022	0

1

Infantile systemic hyalinosis: Variable grades of severity.

Al Kaissi A, Hilmi M, Betadolova Z, Bouchoucha S, Trofimova S, Shboul M, Rustamov G, Dwera W, Sigl K, Kenis V, Kircher SG. Al Kaissi A, et al. Afr J Paediatr Surg. 2021 Oct-Dec;18(4):224-230. doi: 10.4103/ajps.AJPS_162_20. Afr J Paediatr Surg. 2021. PMID: 34341308 Free PMC article.

2

Skeletal phenotype/genotype in progressive pseudorheumatoid chondrodysplasia.

Al Kaissi A, Kenis V, Jemaa LB, Sassi H, Shboul M, Grill F, Ganger R, Kircher SG. Al Kaissi A, et al. Clin Rheumatol. 2020 Feb;39(2):553-560. doi: 10.1007/s10067-019-04783-z. Epub 2019 Oct 18. Clin Rheumatol. 2020. PMID: 31628567

3

Clinical Phenotype and Bone Biopsy Characteristics in a Child with Proteus Syndrome.

Al Kaissi A, Misof BM, Laccone F, Blouin S, Roschger P, Kircher SG, Shboul M, Mindler GT, Girsch W, Ganger R. Al Kaissi A, et al. Calcif Tissue Int. 2021 Nov;109(5):586-595. doi: 10.1007/s00223-021-00862-z. Epub 2021 May 18. Calcif Tissue Int. 2021. PMID: 34003338

4

Novel subtype of mucopolysaccharidosis caused by arylsulfatase K (ARSK) deficiency.

Verheyen S, Blatterer J, Speicher MR, Bhavani GS, Boons GJ, Ilse MB, Andrae D, Sproß J, Vaz FM, Kircher SG, Posch-Pertl L, Baumgartner D, Lübke T, Shah H, Al Kaissi A, Girisha KM, Plecko B. Verheyen S, et al. Among authors: al kaissi a. J Med Genet. 2021 Dec 16:jmedgenet-2021-108061. doi: 10.1136/jmedgenet-2021-108061. Online ahead of print. J Med Genet. 2021. PMID: 34916232 Free article.

5

Schmid's Type of Metaphyseal Chondrodysplasia: Diagnosis and Management.

Al Kaissi A, Ghachem MB, Nabil NM, Kenis V, Melchenko E, Morenko E, Grill F, Ganger R, Kircher SG. Al Kaissi A, et al. Orthop Surg. 2018 Aug;10(3):241-246. doi: 10.1111/os.12382. Epub 2018 Jul 19. Orthop Surg. 2018. PMID: 30027601 Free PMC article.

6

Arthrogryposis is a descriptive term, not a specific disease entity: escobar syndrome is an Example.

Al Kaissi A, Ryabykh S, Ochirova P, Bouchoucha S, Kenis V, Shboul M, Ganger R, Grill F, Kircher SG. Al Kaissi A, et al. Minerva Pediatr. 2020 Jun 12. doi: 10.23736/S0026-4946.20.05796-5. Online ahead of print. Minerva Pediatr. 2020. PMID: 32536119

7

Premature osteoarthritis as presenting sign of type II collagenopathy: a case report and literature review.

Husar-Memmer E, Ekici A, Al Kaissi A, Sticht H, Manger B, Schett G, Zwerina J. Husar-Memmer E, et al. Among authors: al kaissi a. Semin Arthritis Rheum. 2013 Feb;42(4):355-60. doi: 10.1016/j.semarthrit.2012.05.002. Epub 2012 Jun 19. Semin Arthritis Rheum. 2013. PMID: 22717203 Review.

8

Leri-Weill Dyschondrosteosis Syndrome: Analysis via 3DCT Scan.

Al Kaissi A, Shboul M, Kenis V, Grill F, Ganger R, Kircher SG. Al Kaissi A, et al. Medicines (Basel). 2019 May 29;6(2):60. doi: 10.3390/medicines6020060. Medicines (Basel). 2019. PMID: 31146331 Free PMC article.

9

Progressive Deformity of the Lower Limbs in a Patient with KID (Keratitis-Ichthyosis-Deafness) Syndrome.

Kozhevnikov O, Kralina S, Yurasova Y, Kenis V, Kircher SG, Al Kaissi A. Kozhevnikov O, et al. Among authors: al kaissi a. Case Rep Orthop. 2020 Jul 10;2020:8747392. doi: 10.1155/2020/8747392. eCollection 2020. Case Rep Orthop. 2020. PMID: 32733727 Free PMC article.

10

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

Al Kaissi A, Windpassinger C, Chehida FB, Ghachem MB, Nassib NM, Kenis V, Melchenko E, Morenko E, Ryabykh S, Hofstaetter JG, Grill F, Ganger R, Kircher SG. Al Kaissi A, et al. Medicine (Baltimore). 2017 Sep;96(35):e7863. doi: 10.1097/MD.0000000000007863. Medicine (Baltimore). 2017. PMID: 28858097 Free PMC article.

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