M. Tariverdian: search on Z-Library

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1

3D-printed barium strontium titanate-based piezoelectric scaffolds for bone tissue engineering

Tariverdian, Tara, Ghader, Aliasghar Behnam, Milan, Peiman Brouki, Barzegar-Bafrooei, Hadi, Mozafari, Masoud

Journal:

Ceramics International

Year:

2019

Language:

english

File:

PDF, 2.44 MB

english, 2019

2

Agnathia-otocephaly complex: Report of three cases with involvement of two different Carnegie stages

Christiane Schiffer, Gholamali Tariverdian, Monika Schiesser, Mary C. Thomas, Consolato Sergi

Journal:

American Journal of Medical Genetics Part A

Year:

2002

Language:

english

File:

PDF, 140 KB

english, 2002

3

Chromosom 8p-Syndrom: Herzfehler und psycho- motorische Retardierung als Leitsymptome Fallbericht

Stephanie Spranger, Anna Jauch, Inge Rauterberg-Ruland, G. Tariverdian, D. Hager

Journal:

Monatsschrift Kinderheilkunde

Year:

1997

Language:

german

File:

PDF, 235 KB

german, 1997

4

MIDAS-Syndrom – Eine X-chromosomale Erkrankung Differentialdiagnose zum kongenitalen Varizellensyndrom

Stephanie Spranger, H. Stute, A. Blankenagel, A. Jauch, D. Hager, G. Tariverdian

Journal:

Monatsschrift Kinderheilkunde

Year:

1998

Language:

german

File:

PDF, 262 KB

german, 1998

5

Survival up to age 10 years in a patient with partial duplication 6q: case report and review of the literature

Seel, Cornelia, Hager, Hans-Dieter, Jauch, Anna, Tariverdian, Gholamali, Zschocke, Johannes

Journal:

Clinical Dysmorphology

Year:

2005

Language:

english

File:

PDF, 133 KB

english, 2005

6

Holoprosencephaly, bilateral cleft lip and palate and ectrodactyly: another case and follow up

K??nig, Rainer, Beeg, Thomas, Tariverdian, Gholamali, Scheffer, Hans, Bitter, Klaus

Journal:

Clinical Dysmorphology

Year:

2003

Language:

english

File:

PDF, 267 KB

english, 2003

7

Bilateral radial deficiency with lower limb involvement

Spranger, Stephanie, Weber, Michael, Tröger, Jochen, Tariverdian, Gholamali, Opitz, John M.

Journal:

American Journal of Medical Genetics

Year:

1996

File:

PDF, 489 KB

1996

8

Severe mental retardation and macroorchidism without mutation in the FMR1 gene

Reyniers, Edwin, Wolff, Gerhard, Tariverdian, Gholamali, De Boulle, Kristel, Storm, Katrien, Kooy, R. Frank, Willems, Patrick J.

Journal:

American Journal of Medical Genetics

Year:

1996

Language:

english

File:

PDF, 533 KB

english, 1996

9

Short-rib-polydactyly syndrome type Verma-Naumoff-Le Marec in a fetus with histological hallmarks of type Saldino-Noonan but lacking internal organ abnormalities

Hentze, Sabine, Sergi, Consolato, Troeger, Jochen, Revell, Peter A., Otto, Herwart F., Tariverdian, Gholamali

Journal:

American Journal of Medical Genetics

Year:

1998

Language:

english

File:

PDF, 498 KB

english, 1998

10

Rare dental abnormalities seen in oculo-facio-cardio-dental (OFCD) syndrome: three new cases and review of nine patients

Schulze, Birgit R.B., Horn, Denise, Kobelt, Albrecht, Tariverdian, Gholamali, Stellzig, Angelika

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 397 KB

english, 1999

11

L�ri-Weill syndrome as part of a contiguous gene syndrome at Xp22.3

Spranger, Stephanie, Schiller, Simone, Jauch, Anna, Wolff, Kathrin, Rauterberg-Ruland, Inge, Hager, Dieter, Tariverdian, Gholamali, Tr�ger, Jochen, Rappold, Gudrun

Journal:

American Journal of Medical Genetics

Year:

1999

Language:

english

File:

PDF, 249 KB

english, 1999

12

A case of Perlman syndrome: Fetal gigantism, renal dysplasia, and severe neurological deficits

Schilke, Kathrin, Schaefer, Franz, Waldherr, R�diger, Rohrschneider, Wiltrud, John, Christoph, Himbert, Urban, Mayatepek, Ertan, Tariverdian, Gholamali

Journal:

American Journal of Medical Genetics

Year:

2000

Language:

english

File:

PDF, 470 KB

english, 2000

13

Misclassification risk of patients with bilateral cleft lip and palate and manifestations of median facial dysplasia: A new variant of del(22q11.2) syndrome?

Birgit R. B. Schulze, Gholamali Tariverdian, Gerda Komposch, Angelika Stellzig

Journal:

American Journal of Medical Genetics Part A

Year:

2001

Language:

english

File:

PDF, 258 KB

english, 2001

14

Mental retardation, acromegalic face, and megalotestes in two half-brothers: A specific form of X-linked mental retardation without fra(X) (q)?

G. Tariverdian, U. Froster-Iskenius, G. Deuschl, G. Wolff

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 849 KB

english, 1991

15

Tapetoretinal degeneration in brothers with apparent Cohen syndrome: Nosology with Mirhosseini-Holmes-Walton syndrome

Dr. O. Steinlein, G. Tariverdian, H. U. Boll, F. Vogel

Journal:

American Journal of Medical Genetics Part A

Year:

1991

Language:

english

File:

PDF, 445 KB

english, 1991

16

Two sisters with Escobar syndrome

Stephanie Spranger, Matthias Spranger, Hans-Michael Meinck, Gholamali Tariverdian

Journal:

American Journal of Medical Genetics Part A

Year:

1995

Language:

english

File:

PDF, 455 KB

english, 1995

17

Trisomy 8q and partial trisomy 22 in a 43-year-old man with moderate intellectual disability, epilepsy and large cell non-Hodgkin lymphoma

Ingo Helbig, Michael Wirtenberger, Anna Jauch, Hans-Dieter Hager, Gholamali Tariverdian, Kari Hemminki, Barbara Burwinkel, Ruediger Klaes

Journal:

American Journal of Medical Genetics Part A

Year:

2006

Language:

english

File:

PDF, 181 KB

english, 2006

18

Quality of life after restorative proctocolectomy for ulcerative colitis: Preoperative status and long-term results

Mirjam Tariverdian, Christine Leowardi, Ulf Hinz, Thilo Welsch, Jan Schmidt, Peter Kienle

Journal:

Inflammatory Bowel Diseases

Year:

2007

Language:

english

File:

PDF, 202 KB

english, 2007

19

Beta2-microglobulin mutations in microsatellite unstable colorectal tumors

Matthias Kloor, Sara Michel, Boris Buckowitz, Josef Rüschoff, Reinhard Büttner, Elke Holinski-Feder, Wolfgang Dippold, Rudolf Wagner, Mirjam Tariverdian, Axel Benner, Yvette Schwitalle, Beate Kuchenbu

Journal:

International Journal of Cancer

Year:

2007

Language:

english

File:

PDF, 362 KB

english, 2007

20

Agnathia-otocephaly complex: presentation of four cases

C. Schiffer, G. Tariverdian, M. Schiesser, C. Sergi

Journal:

Pathology - Research and Practice

Year:

2004

Language:

english

File:

PDF, 147 KB

english, 2004

21

Molecular analysis of aniridia patients for deletions involving the Wilms' tumor gene

M. Drechsler, E. J. Meijers-Heijboer, S. Schneider, B. Schurich, C. Grond-Ginsbach, G. Tariverdian, G. Kantner, A. Blankenagel, D. Kaps, T. Schroeder-Kurth, B. Royer-Pokora

Journal:

Year:

1994

Language:

english

File:

PDF, 1015 KB

english, 1994

22

Molecular analysis of mutations in the gene FMR-1 segregating in fragile X families

P. Steinbach, D. Wöhrle, G. Tariverdian, I. Kennerknecht, G. Barbi, H. Edlinger, H. Enders, M. Götz-Sothmann, H. Heilbronner, D. Hosenfeld, R. Kircheisen, F. Majewski, P. Meinecke, E. Passarge, A. Sch

Journal:

Year:

1993

Language:

english

File:

PDF, 1.47 MB

english, 1993

23

Genetics and linkage analysis of adenosine deaminase

H. Ritter, G. G. Wendt, G. Tariverdian, J. Zilch, M. Rube, G. Kirchberg

Journal:

Year:

1971

Language:

english

File:

PDF, 150 KB

english, 1971

24

Genetic and linkage analysis on 6-PGD

H. Ritter, G. Tariverdian, G. G. Wendt, I. Zilch

Journal:

Year:

1971

Language:

english

File:

PDF, 96 KB

english, 1971

25

A monozygotic twin pair with Rett syndrome

G. Tariverdian, Gisela Kantner, F. Vogel

Journal:

Year:

1987

Language:

english

File:

PDF, 798 KB

english, 1987

26

Genetics and linkage analysis on phosphoglucomutase

G. G. Wendt, H. Ritter, I. Zilch, G. Tariverdian, G. Utermann, I. Kindermann, G. Kirchberg

Journal:

Year:

1971

Language:

english

File:

PDF, 113 KB

english, 1971

27

Genetics and linkage analysis on adenylate kinase

G. G. Wendt, H. Ritter, I. Zilch, G. Tariverdian, I. Kindermann, G. Kirchberg

Journal:

Year:

1971

Language:

english

File:

PDF, 92 KB

english, 1971

28

Zur transspezifischen Variabilität der 6-Phosphogluconatdehydrogenase (E.C.: 1.1.1.44) der Primaten

G. Tariverdian, H. Ritter, J. Schmitt

Journal:

Year:

1971

File:

PDF, 240 KB

1971

29

Evidence for linkage between the locus for the AB0-system and the locus for phosphoglucoseisomerase (PGI)

H. Ritter, G. Tariverdian, H. Arnold, K. G. Blume, W. Schröter, E. Zimmerschitt, G. Brittinger, E. König, G. G. Wendt

Journal:

Year:

1971

Language:

english

File:

PDF, 77 KB

english, 1971

30

Zur transspezifischen Variabilität der NAD-Malatdehydrogenase (E.C.: 1.1.1.37) der Primaten

G. Tariverdian, H. Ritter, J. Schmitt

Journal:

Year:

1971

File:

PDF, 130 KB

1971

31

Erythrocytenenzyme der Primaten

G. Tariverdian, H. Ritter, J. Schmitt

Journal:

Year:

1971

File:

PDF, 190 KB

1971

32

Zur Genetik der 6-Phosphogluconatdehydrogenase (EC: 1.1.1.44): Eine neue Variante F (Freiburg)

G. Tariverdian, H. Ropers, J. Op't Hof, H. Ritter

Journal:

Year:

1970

File:

PDF, 123 KB

1970

33

Down's syndrome in twins with discordant HL-A phenotypes

W. Hirsch, K. Bender, A. Mayerova, H. Riehm, H. Ritter, G. Tariverdian

Journal:

Year:

1974

Language:

english

File:

PDF, 1.01 MB

english, 1974

34

Nonspecific X-linked mental retardation—A review

Gholamali Tariverdian, Barbara Weck

Journal:

Year:

1982

Language:

english

File:

PDF, 2.71 MB

english, 1982

35

Prenatal enzymatic diagnosis and exclusion of Krabbe's disease (globoid-cell leukodystrophy) using chorionic villi in five risk pregnancies

K. Harzer, H. -D. Hager, G. Tariverdian

Journal:

Year:

1987

Language:

english

File:

PDF, 298 KB

english, 1987

36

Transspecific variability of phosphohexose isomerase (E. C.: 5. 3. 1. 9) in primates

G. Tariverdian, H. Ritter, J. Schmitt

Journal:

Year:

1971

Language:

english

File:

PDF, 346 KB

english, 1971

37

The secretor locus as a marker for prenatal prediction of myotonic dystrophy (DM)

J. Greiner, D. H. Spengler, J. Krüger, G. Tariverdian

Journal:

Year:

1988

Language:

english

File:

PDF, 249 KB

english, 1988

38

Zur Formalgenetik der Phosphoglucoseisomerase (EC: 5.3.1.9)

G. Tariverdian, H. Arnold, K. G. Blume, U. Lenkeit, G. W. Löhr

Journal:

Year:

1970

File:

PDF, 277 KB

1970

39

Genetisch kontrollierte Varianten der NADH-Diaphorase

G. Tariverdian, H. Ritter, G. G. Wendt

Journal:

Year:

1970

File:

PDF, 127 KB

1970

40

Erythrocytenenzyme der Primaten

J. Schmitt, G. Tariverdian, H. Ritter

Journal:

Year:

1971

File:

PDF, 155 KB

1971

41

Zur populationsgenetik der phosphoglucoseisomerase (EC: 5.3.1.9)

G. Tariverdian, H. Obracaj, H. Ritter, G. G. Wendt

Journal:

Year:

1971

File:

PDF, 92 KB

1971

42

Zur transspezifischen Variabilität der NADH-Diaphorase der Primaten

J. Schmitt, G. Tariverdian, H. Ritter

Journal:

Year:

1971

File:

PDF, 241 KB

1971

43

Zur Populationsgenetik der Phosphohexoseisomerasen (EC: 5.3.1.9) beim Schwein

Journal:

Year:

1970

File:

PDF, 143 KB

1970

44

Case report

S. Spranger, G. Tariverdian, F. K. Albert, D. Sontheimer, J. Zöller, M. Weber, J. Tröger

Journal:

European Journal of Pediatrics

Year:

1996

Language:

english

File:

PDF, 1.18 MB

english, 1996

45

Unique occurrence of Brachmann-de lange syndrome in a fetus whose mother presented with a diffuse large B-cell lymphoma

Christiane Schiffer, Monika Schiesser, Jutta Lehr, Gholamali Tariverdian, Dieter Glaeser, Heinz Gabriel, Gregor Mikuz, Consolato Sergi

Journal:

Pathology & Oncology Research

Year:

2007

Language:

english

File:

PDF, 156 KB

english, 2007

46

Neuroendocrine circuitry and endometriosis: progesterone derivative dampens corticotropin-releasing hormone-induced inflammation by peritoneal cells in vitro

Nadja Tariverdian, Mirjam Rücke, Julia Szekeres-Bartho, Sandra M. Blois, Eva F. Karpf, Peter Sedlmayr, Burghard F. Klapp, Heribert Kentenich, Friederike Siedentopf, Petra C. Arck

Journal:

Journal of Molecular Medicine

Year:

2010

Language:

english

File:

PDF, 392 KB

english, 2010

47

Ellis-van Creveld syndrome: a generalized dysplasia of enchondral ossification

C. Sergi, Theda Voigtländer, Saida Zoubaa, Sabine Hentze, Gabriele Meyberg-Solomeyer, Jochen Troeger, Gholamali Tariverdian, Herwart F. Otto, Monika Schiesser

Journal:

Pediatric Radiology

Year:

2001

Language:

english

File:

PDF, 253 KB

english, 2001

48

Neuroendocrine–immune disequilibrium and endometriosis: an interdisciplinary approach

Nadja Tariverdian, Theoharis C. Theoharides, Friederike Siedentopf, Gabriela Gutiérrez, Udo Jeschke, Gabriel A. Rabinovich, Sandra M. Blois, Petra C. Arck

Journal:

Seminars in Immunopathology

Year:

2007

Language:

english

File:

PDF, 447 KB

english, 2007

49

Long-term outcome 10

Christine Leowardi, Ulf Hinz, Mirjam Tariverdian, Peter Kienle, Christian Herfarth, Alexis Ulrich, Martina Kadmon

Journal:

Langenbeck's Archives of Surgery

Year:

2010

Language:

english

File:

PDF, 160 KB

english, 2010

50

Maternal uniparental disomy 7 – review and further delineation of the phenotype

D. Kotzot, D. Balmer, A. Baumer, K. Chrzanowska, B. C. J. Hamel, H. Ilyina, M. Krajewska-Walasek, I. W. Lurie, B. J. Otten, E. Schoenle, G. Tariverdian, A. Schinzel

Journal:

European Journal of Pediatrics

Year:

2000

Language:

english

File:

PDF, 410 KB

english, 2000