Abdul A Al Saadi: Influence Statistics

Abdul A Al Saadi

Abdul A Al Saadi

Department of Pediatrics, William Beaumont Hospital, Royal Oak, Michigan 48072-2735. | Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, MI, USA | ...

Abdul A Al Saadi: Expert Impact

Concepts for which Abdul A Al Saadi has direct influence: Renal dysplasia , Ataxia telangiectasia , Cell hyperplasia , Partial trisomy , Triploidy syndrome , Chromosomal abnormalities , Cytogenetic studies .

Abdul A Al Saadi: KOL impact

Concepts related to the work of other authors for which for which Abdul A Al Saadi has influence: Medullary thyroid carcinoma , Multiple endocrine , Cell hyperplasia , Thyroid gland , Ataxia telangiectasia , Neoplasia type , Human pair .

KOL Resume for Abdul A Al Saadi

Year
1989

Department of Pediatrics, William Beaumont Hospital, Royal Oak, Michigan 48072-2735.

1987

Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, MI, USA

1984

Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, Michigan

1980

Department of Internal Medicine, William Beaumont Hospital, 48072, Royal Oak, Michigan, USA

1976

Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak. Michigan, USA.

Prominent publications by Abdul A Al Saadi

KOL-Index: 7295 . Cytogenetic study of 45 meningiomas from 31 female and 14 male patients are reported. No chromosomal abnormalities were found in nine (20%). These were predominantly meningotheliomatous, and were from younger patients (average age, 46 years). Monosomy 22 was noted in only 20% and in 12 patients (27%) with other losses and rearrangements. Among the latter, 50% were either recurrent or ...
Known for Cytogenetic Studies | Clinical Significance | Human Brain Tumors | Chromosomal Abnormalities
KOL-Index: 6299 . Sequential cytogenetic studies of four patients with ataxia telangiectasia showed the progressive development of lymphocyte clones, each marked with a rearranged chromosome 14. Initial studies had shown random chromosomal breaks and rearrangements. Later studies in all patients showed nonrandom rearrangement of chromosome 14 with a breakpoint at 14q12 and with the distal segment ...
Known for Ataxia Telangiectasia | Chromosomal Abnormalities | Cytogenetic Studies | 1315 Chromosomes Human
KOL-Index: 5267 . A newborn with severely shortened ribs, short limbs, and postaxial polydactyly died shortly after birth. Postmortem roentgenograms established the diagnosis of type 3 short rib-polydactyly (SRP) syndrome as described by Naumoff and associates. Histopathologic study showed the chondrocytes to contain previously undescribed cytoplasmic inclusion bodies that were PAS-positive and ...
Known for Type 3 | Short Rib‐polydactyly Syndrome | Cardiac Malformations | Reported Cases
KOL-Index: 4981 . Two sisters at risk for hereditary medullary carcinoma and having small but progressive increases of serum calcitonin in response to calcium infusion underwent thyroidectomy. The thyroid glands were studied for C-cell distribution. Middle and upper portions of the lateral thyroid lobes showed marked increases and clustering of calcitonin-containing cells in comparison with normal thyroid ...
Known for Thyroid Carcinoma | Cell Hyperplasia | Precancerous Conditions | Serum Calcitonin
KOL-Index: 4631 . A term infant had dwarfism with characteristic skeletal and extraskeletal changes of the short rib-polydactyly syndrome type 2 (Majewski). The skeletal changes included extremely short horizontal ribs, extreme micromelia with disproportionately short ovoid tibiae, and pre- and post-axial polydactyly. Microscopically, cartilage showed markedly stunted and disorganized endochondral ...
Known for Multiple Bone Diseases | Polydactyly Syndrome | Majewski Type | Recessive Humans Infant
KOL-Index: 3872 . C cell hyperplasia and occult medullary carcinoma of the thyroid in asymptomatic individuals at genetic risk can be detected by measurement of serum calcitonin concentrations before and after stimulation with a secretagogue. Electron microscopy was used to confirm the presence of C cell hyperplasia afte demonstration of elevated serum calcitonin values in three asymptomatic young women ...
Known for Cell Hyperplasia | Medullary Thyroid | Calcitonin Carcinoma | Neoplasms Adolescent
KOL-Index: 3578 . A baby with partial trisomy 7, 46, XY,t (5;7) (q35;q31) resulting from a familial translocation (5q+,7q-) is reported. The clinical abnormalities of this case closely resemble those of previously reported cases of partial trisomy 7. It is suggested that partial trisomy 7 may represent a clinical entity.
Known for Partial Trisomy | Long Arm | Chromosome 7 | Familial Translocation
KOL-Index: 3571 . A family study was undertaken to investigate genetic involvement in renal dysplasia, which is defined as abnormal metanephric differentiation. Probands were ascertained through the retrospective examination of necropsy records and the reevaluation of available material, which included microscopic examinations of the kidneys, gross descriptions of organs, and gross photographs. We obtained ...
Known for Renal Dysplasia | Urethral Valves | Publication Abnormalities | Newborn Kidney
KOL-Index: 3208 . Two live-born cases, 69,XXY and one stillbirth, 69,XXX are reported. Further evidence is presented to delineate the triploidy syndrome. Common external and internal features which characterize the triploidy syndrome are low-set ears, hypertelorism, colobomata, syndactyly, simian creases, microphallus, undescended testes, scrotal aplasia, anomalous heart and hypoplasia of kidneys and ...
Known for Triploidy Syndrome | Publication Abnormalities | Chromosome Aberrations | Congenital Humans
KOL-Index: 3007
Known for Interstitial Deletion | Chromosome 18 | Human Pair | Abnormal Behaviour
KOL-Index: 531
Known for Cartilage Cells | Humans Karyotyping | Bone Diseases

Key People For Renal Dysplasia

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Department of Pediatrics, William Beaumont Hospital, Royal Oak, Michigan 48072-2735. | Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, MI, USA | Department of Anatomic Pathology, William Beaumont Hospital, Royal Oak, Michigan