Rezultatet e kërkimit

BRUGADA SYNDROME 3 ; TIMOTHY SYNDROME-LONG QT | N/A | ANAA2926
CARDIOMYOPATHY, HYPERTROPHIC, 24 | N/A | ANAA2972
PREIMPLANTATION GENETIC DIAGNOSIS (PGD) COUPLED TO HLA MATCHING FOR A SINGLE GENE DISORDER From 1 to 10 embryos | N/A | ANAA2994
11EKDELC MUTATION OF THE CHEK2 GENE + DELETION / DUPLICATION ANALYSIS | N/A | ANAA2890
15q13.3 MICRODELETION SYNDROME | N/A | ANAA2833
15q24 MICRODELETION SYNDROME | N/A | ANAA2834
15q26 MICRODELETION SYNDROME | N/A | ANAA2842
16p11 MICRODELETION SYNDROME | N/A | ANAA2835
17q12 MICRODELETION SYNDROME | N/A | ANAA2837
17q21.31 MICRODELETION SYNDROME | N/A | ANAA2838
18q21.2 (Pitt-Hopkins) MICRODELETION SYNDROME | N/A | ANAA2839
1p36 MICRODELETION SYNDROME | N/A | ANAA2821
1q21.1 (TAR) MICRODELETION SYNDROME | N/A | ANAA2822
22q13 MICRODELETION SYNDROME | N/A | ANAA2840
2p16.1 MICRODELETION SYNDROME | N/A | ANAA2823
3-hydroxyisobutryl-CoA hydrolase deficiency | N/A | ANAA2756
35delG CONNEXIN 26 GENE MUTATION (NONSYNDROMIC HEARING LOSS) | N/A | ANAA2110
3q29 MICRODELETION SYNDROME | N/A | ANAA2824
7q36.1 MICRODELETIONS SYNDROME | N/A | ANAA2829
9q22.3 MICRODELETION SYNDROME | N/A | ANAA2831
A-DHE B- THALASSAEMIA | N/A | ANAA2122
A-THALASSAEMIA | N/A | ANAA2121
ACHONDROPLASIA (FGFR3 GENE) | N/A | ANAA2797
Acrokeratosis verruciformis | N/A | ANAA2233
ACROMESOMELIC DYSPLASIA – HUNTER – THOMPSON TYPE | N/A | ANAA2906
ACROMESOMELIC DYSPLASIA, HUNTER-THOMPSON TYPE | N/A | ANAA2812
aFP LEVELS IN THE AMNIOTIC FLUID | N/A | ANAA2366
Albinism, oculocutaneous, type IA | N/A | ANAA2235
Albinism, oculocutaneous, type II | N/A | ANAA2234
Alopecia universalis | N/A | ANAA2236
Alport syndrome | N/A | ANAA2762
Alzheimer's disease risk assessment (AD2) - E4 allele (late onset) | N/A | ANAA2788
ALZHEIMER'S DISEASE, LATE ONSET (AD2) | N/A | ANAA2979
AML1/ETO HYBRID GENE DETECTION-SEMIQUANTITATIVE ANALYSIS | N/A | ANAA2878
AMPLIFICATION 21q22.1 detected by MLPA | N/A | ANAA2881
AORTIC ANEURYSM, FAMILIAL THORACIC 4 | N/A | ANAA2942
AORTIC ANEURYSM, FAMILIAL THORACIC 6 | N/A | ANAA2944
AORTIC ANEURYSM, FAMILIAL THORACIC 7 | N/A | ANAA2943
APERT SINDROME | N/A | ANAA2801
Argininosuccinic aciduria | N/A | ANAA2746
ARIOSA ( HARMONY PRENATAL TEST ) (TRISOMIA 21;18;13 + FETAL SEX + ANEUPLOIDITE XY) | N/A | ANAA2109
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA 10 | N/A | ANAA2947
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA 11 WITH MILD PALMOPLANTAR KERATODERMA AND WOOLLY HAIR | N/A | ANAA2948
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA 2 | N/A | ANAA2945
ARRHYTHMOGENIC RIGHT VENTRICULAR DYSPLASIA 9 | N/A | ANAA2946
ATRIAL SEPTAL DEFECT 2 | N/A | ANAA2960
B-CELL CLONALITY ANALYSIS | N/A | ANAA2897
B-THALASSAEMIA DHE SICKLE-CELL ANAEMIA (DREPANOCITOZA) | N/A | ANAA2120
BCR/ABL HYBRID GENE DETECTION-SEMIQUANTITATIVE ANALYSIS | N/A | ANAA2876
BEARE – STEVENSON SYNDROME | N/A | ANAA2844
BEARE-STEVENSON SYNDROME | N/A | ANAA2813
Biotinidase deficiency | N/A | ANAA2747
BRAF GENE – BRAF V600E & V600K MUTATIONS | N/A | ANAA2907
BRAF V600E + BRAF V600K Mutations | N/A | ANAA2882
BREAST + OVARIAN CANCER – 19 GENE (PERFSHIRE BRCA1 + BRCA2) – NGS PANEL, Genomic Testing | N/A | ANAA2899
BREAST AND OVARIAN CANCER, BRCA1 + BRCA2 GENE | N/A | ANAA2900
BRUGADA SYNDROME - 8 GENES MINIMAL NGS PANEL - GENOMIC TESTING | N/A | ANAA2923
BRUGADA SYNDROME 1; LONG QT SYNDROME-3; SICK SINUS SYNDROME 1 | N/A | ANAA2924
BRUGADA SYNDROME 2 | N/A | ANAA2925
BRUGADA SYNDROME 4 | N/A | ANAA2927
BRUGADA SYNDROME 5 | N/A | ANAA2928
BRUGADA SYNDROME 6 | N/A | ANAA2929
BRUGADA SYNDROME 7 | N/A | ANAA2930
BRUGADA SYNDROME 8 | N/A | ANAA2931
CAMPOMELIC DYSPLASIA | N/A | ANAA2811
CARDIAC ARRHYTHMIAS - 40 GENES NGS PANEL - GENOMIC TESTING | N/A | ANAA2921
Cardiomyopathy (mutations A3243G, A4269G, A4300G | N/A | ANAA2352
CARDIOMYOPATHY, DILATED, 1AA, WITH OR WITHOUT LVNC | N/A | ANAA2950
CARDIOMYOPATHY, DILATED, 1D | N/A | ANAA2951
CARDIOMYOPATHY, DILATED, 1EE | N/A | ANAA2952
CARDIOMYOPATHY, DILATED, 1HH | N/A | ANAA2953
CARDIOMYOPATHY, DILATED, 1NN; NOONAN SYNDROME 5; LEOPARD SYNDROME 2 | N/A | ANAA2956
CARDIOMYOPATHY, DILATED, 1O | N/A | ANAA2958
CARDIOMYOPATHY, DILATED, 1S | N/A | ANAA2954
CARDIOMYOPATHY, DILATED, 1Z | N/A | ANAA2955
CARDIOMYOPATHY, DILATED, 2A | N/A | ANAA2957
CARDIOMYOPATHY, HYPERTROPHIC 6 | N/A | ANAA2964
CARDIOMYOPATHY, HYPERTROPHIC, 10 | N/A | ANAA2966
CARDIOMYOPATHY, HYPERTROPHIC, 11 | N/A | ANAA2967
CARDIOMYOPATHY, HYPERTROPHIC, 15 | N/A | ANAA2968
CARDIOMYOPATHY, HYPERTROPHIC, 16 | N/A | ANAA2969
CARDIOMYOPATHY, HYPERTROPHIC, 18 | N/A | ANAA2970
CARDIOMYOPATHY, HYPERTROPHIC, 19 | N/A | ANAA2971
CARDIOMYOPATHY, HYPERTROPHIC, 3 | N/A | ANAA2962
CARDIOMYOPATHY, HYPERTROPHIC, 4 | N/A | ANAA2963
CARDIOMYOPATHY, HYPERTROPHIC, 8 | N/A | ANAA2965
CarrierFree ®- carrier analysis in a future parent for more than 330 recessive gene disorders using DNA sequencing of all exons of 277 genes | N/A | ANAA2997
CHARCOT MARIE TOOTH 1A (CMT1A) and HNPP | N/A | ANAA2782
CHARCOT MARIE TOOTH CMTX1 (Sex-linked) | N/A | ANAA2783
CHARCOT-MARIE-TOOTH (CMT) - 42 GENES NGS PANEL - GENOMIC TESTING | N/A | ANAA2784
CHIMERISM AFTER TRANSPLANTATION | N/A | ANAA2982
Chondrosarcoma | N/A | ANAA2745
Ciliary dyskinesia, primary 3, with or without situs inversus | N/A | ANAA2264
Ciliary dyskinesia, primary 7, with or without situs inversus | N/A | ANAA2265
Ciliary dyskinesia, primary 9, with or without situs inversus | N/A | ANAA2266
Ciliary dyskinesia, primary, 11 | N/A | ANAA2267
Ciliary dyskinesia, primary, 12 | N/A | ANAA2268
Ciliary dyskinesia, primary, 15 | N/A | ANAA2270
Ciliary dyskinesia, primary, 6 | N/A | ANAA2252
Citrullinemia, type II, neonatal-onset | N/A | ANAA2748
Combined immunodeficiency, X-linked, moderate | N/A | ANAA2742
COWDEN SYNDROME - ???? HAMARTOMA TUMOR SYNDROME | N/A | ANAA2916
CPEO syndrome (mutations A3243G, T4274C) | N/A | ANAA2350
CRI DU CHAT SYNDROME | N/A | ANAA2826
CROUZON SINDROME WITH ACANTHOSIS NIGRICANS | N/A | ANAA2799
CROUZON SYNDROME | N/A | ANAA2798
Cystinosis, nephropathic | N/A | ANAA2763
D8 MUTATIONS 35Y AND ITD OF THE FLT3 GENE | N/A | ANAA2880
D835Y AND ITD MUTATIONS OF THE FLT3 GENE | N/A | ANAA2896
DELETION 17p12.2 | N/A | ANAA2868
DELETION 5q33-q35 | N/A | ANAA2866
DELETION 6q25-q26 | N/A | ANAA2867
DELETION 3q27 FISH | N/A | ANAA2865
DELETION OF 10q23 | N/A | ANAA2871
DELETION OF 11q22.3 | N/A | ANAA2872
DELETION OF 12p13.2 | N/A | ANAA2875
DELETION OF 13q14 | N/A | ANAA2873
DELETION OF 17p13 | N/A | ANAA2874
DELETION OF 9p21.3 | N/A | ANAA2870
DELETION/DUPLICATION OF 8q24 | N/A | ANAA2869
DETECTION OF 35delG MUTATION | N/A | ANAA2126
DETECTION OF THE CDNA GENE MUTATION D816V | N/A | ANAA2886
DETECTION OF THE S505 AND W515 MUTATIONS OF THE MPL GENE | N/A | ANAA2887
Diabetes and hearing loss (A3243G, C12258A) | N/A | ANAA2353
DIAMOND - BLACKFAN ANEMIA 7 GENES – Genomic Testing | N/A | ANAA2849
DIGEORGE/VCFS/CAT EYE SYNDROME | N/A | ANAA2841
Dihydrolipoamide dehydrogenase deficiency | N/A | ANAA2754
DNA EXTRACTION AND BANKING FOR FUTURE INVESTIGATION | N/A | ANAA2983
DONOSAFE ® - DNA SEQUENCING OF ALL EXONS OF 285 GENES - GENETIC DISEASES | N/A | ANAA2999
DOWN SYNDROME USING BIOCHEMICAL MARKERS + F508del CFTR GENE MUTATION OF CYSTIC FIBROSIS + 35delG CONNEXIN26 GENE MUTATION ( NONSYNDROMIC HEARING LOSS ) | N/A | ANAA2113
DOWN SYNDROME USING BIOCHEMICAL MARKERS AND DETECTION F508del CFTR GENE MUTATION OF CYSTIC FIBROSIS | N/A | ANAA2112
DUCHENNE / BECKER (DMD/BMD) MUSCULAR DYSTROPHY | N/A | ANAA2774
DUCHENNE/BECKER(DMD/BMD) MUSCULAR DYSTROPHY, EXTENDED TEST | N/A | ANAA2775
DUPLICATION 2p24 FISH | N/A | ANAA2864
EARLY-ONSET FAMILIAL ALZHEIMER DISEASE TYPE 1 (AD1) | N/A | ANAA2787
EARLY-ONSET FAMILIAL ALZHEIMER DISEASE TYPE 3 (AD3) | N/A | ANAA2786
Ehlers-Danlos classic type | N/A | ANAA2769
EHLERS-DANLOS SYNDROME - 7 GENES MINIMAL NGS PANEL - GENOMIC TESTING | N/A | ANAA2809
Ehlers-Danlos syndrome due to tenascin X deficiency | N/A | ANAA2771
Ehlers-Danlos syndrome, type III | N/A | ANAA2768
Ehlers-Danlos syndrome, type VI | N/A | ANAA2770
Encephalomyopathy (G1606A, T10010C) | N/A | ANAA2354
Epilepsy 332 genes NGS panel - Genomic testing | N/A | ANAA2791
EXPANSION OF THE ERBB2 GENE (HER2-NEU AMPLIFICATION) | N/A | ANAA2885
F508del CFTR GENE MUTATION OF CYSTIC FIBROSIS AND 35delG CONNEXIN26 GENE MUTATION (NONSYNDROMIC HEARING LOSS) | N/A | ANAA2111
FAKTORI V - LEIDEN G1691A(FVR506Q) + FAKTORI V KOAGULIMIT H1299R (VR2) (FVR 506Q + VR2) | N/A | ANAA2115
FAKTORI XIII – MUTACIONI V34L | N/A | ANAA2118
FAMILIAL ADENOMATOUS POLYPOSIS (FAP) | N/A | ANAA2902
FAMILIAL MEDITERANEAN FEVER ETHET MESDHETARE FAMILJARE | N/A | ANAA2178
FAMILIAL MELANOMA | N/A | ANAA2919
FANCONI ANAEMIA - PERIPHERAL BLOOD LYMPHOCYTE KARYOTYPE ANALYSIS | N/A | ANAA2847
FANCONI ANEMIA 17 GENES – Genomic Testing | N/A | ANAA2848
Fertilitis ® - investigation of male or female infertility usign DNA sequencing of all exons of ~ 160 genes | N/A | ANAA2996
FETALIS – ANALIZE E EMBRIONIT “SEQUENCING ALL EXONS OF 760 GENES” | N/A | ANAA2371
FETALSAFE – ANALIZE E EMBRIONIT “SEQUENCING ALL EXONS OF 800 GENES” | N/A | ANAA2372
FetalSafe ® - analysis of an embryo for more than 800 inherited diseases by DNA sequencing of all exons of ~ 800 genes associated with one of these diseasesoccurred in childhood | N/A | ANAA3005
FIBRINOGJENI POLIMORFIZEM – 455 C >A | N/A | ANAA2977
FIBROZA CISTIKE 87% E MUTACIONEVE TE GENIT CFTR | N/A | ANAA2123
FIBROZA CYSTIKE – Mutacioni F508 del | N/A | ANAA2125
FRAGILE X (FRAXA, FRAXE) SYNDROME in a carrier or an affected individual or in prenatal diagnosis | N/A | ANAA2816
FRIEDREICH ATAXIA | N/A | ANAA2776
GAMETE DONOR – Rutine Genetic Testing | N/A | ANAA2990
GASTROINTESTINAL CANCERS - 21 GENES NGS PANEL - GENOMIC TESTING | N/A | ANAA2912
Genomic testing for Polycystic Kidney Disease PKD1, PKD2 & PKHD1 genes NGS panel with MLPA | N/A | ANAA2761
GENOMIC TESTING FOR SHORT & LONG QT - 12 GENES MINIMAL NGS PANEL | N/A | ANAA2922
Glycogen storage disease II | N/A | ANAA2242
Glycogen storage disease IV | N/A | ANAA2243
HEAMOFILIA A+B GENOMIC TESTING ( F8 & F9 GENES ) | N/A | ANAA2357
HEARING LOSS AND DEAFNESS 122 GENES, NGS PANEL, GENOMIC TESTING | N/A | ANAA2378
Hereditary dementias - 48 genes NGS panel - Genomic testing | N/A | ANAA2793
HEREDITARY DIFFUSE GASTRIC CANCER (HDGC) | N/A | ANAA2918
HEREDITARY NON-POLYPOSIS COLORECTAL CANCER (HNPCC) | N/A | ANAA2901
Hereditary Spastic Paraplegias HSP - 63 genes NGS panel - Genomic testing | N/A | ANAA2794
HUNTINGTON DISEASE | N/A | ANAA2777
HYPERTROPHIC AND DILATED CARDIOMYOPATHIES (HCM & DCM) - 48 GENES NGS PANEL - GENOMIC TESTING | N/A | ANAA2920
Hypophosphatasia, childhood | N/A | ANAA2744
HYPOPLASTIC LEFT HEART SYNDROME 2; TETROLOGY OF FALLOT; VENTRICULAR SEPTAL DEFECT 3 | N/A | ANAA2932
IDENTIFICATION OF PATERNITY USING NON-ROUTINE SAMPLES | N/A | ANAA2975
IDENTIFICATION OF PATERNITY, PRENATAL | N/A | ANAA2974
INVERSION inv(16) FISH | N/A | ANAA2853
JACKSON-WEISS SINDROME | N/A | ANAA2802
JAK2 V617F MUTATION | N/A | ANAA2879
JERVELL AND LANGE-NIELSEN SYNDROME 2; LONG QT SYNDROME 5 | N/A | ANAA2933
JERVELL AND LANGE-NIELSEN SYNDROME; LONG QT SYNDROME 1; SHORT QT SYNDROME 2 | N/A | ANAA2934
KARIOTIPI I GJAKUT PERIFERIK ( HIGH RESOLUTION ) | N/A | ANAA2374
KARIOTIPI I PALCES SE KOCKES | N/A | ANAA2375
KARIOTIPI I PALCES SE KOCKES + MLPA Teknike | N/A | ANAA2376
KARIOTIPI MOLEKULAR I PRODUKTEVE TE ABORTIT | N/A | ANAA2365
KARIOTIPI MOLEKULAR ME HIGH RESOLUTION ? 50 – 100 kb (2 nd level ) | N/A | ANAA2373
KARIOTIPI NGA PALCA E KOCKES | N/A | ANAA2845
KARIOTIPI NGA PRODUKTET E ABORTIT | N/A | ANAA2364
KARIOTIPI PRENATAL NE GJAKUN FETAL | N/A | ANAA2363
KARYOTYPE ANALYSIS OF BONE MARROW CELLS AND MULTIPLE CHROMOSOMAL REARRANGEMENTS (MLPA) | N/A | ANAA2846
KARYOTYPE ANALYSIS OF FIBROBLAST CELLS | N/A | ANAA2367
Kearns-Sayre syndrome | N/A | ANAA2343
KENNEDY (SBMA) DISEASE | N/A | ANAA2778
KRAS – GENI TUMORIAL ONKOGEN + NRAS | N/A | ANAA2908
KROMOZOMI Y MICRODELETIONS ( del Y ) | N/A | ANAA2114
LANGER-GIEDON SYNDROME | N/A | ANAA2830
Leigh syndrome (mutation T8993G/C) | N/A | ANAA2347

Intermedica Qëndrore

Tiranë
Rr. Panorama (Pranë Hipotekës)
Tel.: 042 200 600
Orari: 07:00 – 20:30
E shtunë: 07:30 – 17:00

Intermedica 1

Tiranë
Rr. Reshit Petrela (Përballë Stacionit të Trenit)
Tel.: 04 22 74 662 \ Fax.: 04 22 34 166
Mob.: 068 60 34 558 (recepsioni)
Orari: 07:00 – 20:30
E shtunë: 07:30 – 17:00

Intermedica 2

Tiranë
Rr. “Kongresi i Manastirit”  (Përballë Spitalit Pediatrik)
Tel.: 04 23 78 408
Orari: 07:00 – 20:30
E shtunë: 07:30 – 16:00

Intermedica 3

Tiranë
Rr. Lord Bajron (Përballë Spitalit Ushtarak)
Tel.: 04 23 57 890
Orari: 07:00 – 20:30
E shtunë 07:30 – 16:00

Intermedica 4

Tiranë
Rr. Nazmi Rushiti (Pranë Maternitetit të Ri)
Tel.: 04 23 68 803
Orari: 07:00 – 20:30
E shtunë: 07:30 – 16:00

Intermedica 5

Tiranë
Rr. Zonja Curre (Pranë Tregut Elektrik)
Tel.: 04 22 57 688
Orari: 08:00 – 20:00
E shtunë: Pushim

Intermedica 6 Sarandë

Sarande
Rr. Onhenzmi (Përballë Spitalit “Petro Nako”)
Tel.: 0 85 27 293
Cel.: 069 69 14 776
Orari: 08:00 – 20:00,
E shtunë: 08:00 – 16:00

Intermedica 7

Tiranë
Rruga Fran Bardhi (Pranë Qendrës Kristal)

Tel.: 042 200 600
Orari: 07:00 – 20:30
E shtunë: 07:30 – 16:00