The Molecular Pathogenesis of Hereditary and Sporadic Adrenocortical and Adrenomedullary Tumors

p53 Mutations in Human Cancers

1991 • 8,133 citations

Germ Line p53 Mutations in a Familial Syndrome of Breast Cancer, Sarcomas, and Other Neoplasms

1990 • 3,720 citations

CONSENSUS: Guidelines for Diagnosis and Therapy of MEN Type 1 and Type 2

2001 • 1,852 citations

Activating Mutations of the Stimulatory G Protein in the McCune–Albright Syndrome

1991 • 1,601 citations

Soft-Tissue Sarcomas, Breast Cancer, and Other Neoplasms

1969 • 1,437 citations

Germ-Line Mutations in Nonsyndromic Pheochromocytoma

2002 • 1,342 citations

Von Recklinghausen Neurofibromatosis

1981 • 1,336 citations

A chimaeric llβ-hydroxylase/aldosterone synthase gene causes glucocorticoid-remediable aldosteronism and human hypertension

1992 • 1,126 citations

Mutations of the gene encoding the protein kinase A type I-α regulatory subunit in patients with the Carney complex

2000 • 1,109 citations

Two G Protein Oncogenes in Human Endocrine Tumors

1990 • 1,038 citations

Comparative histologic study of 43 metastasizing and nonmetastasizing adrenocortical tumors

1984 • 893 citations

The Cellular Functions of Small GTP-Binding Proteins

1990 • 881 citations

Incidentally Discovered Adrenal Masses*

1995 • 853 citations

Tumour predisposition in mice heterozygous for a targeted mutation in Nf1

1994 • 777 citations

Disruption of imprinting caused by deletion of the H19 gene region in mice

1995 • 765 citations

Clinical and Molecular Features of the Carney Complex: Diagnostic Criteria and Recommendations for Patient Evaluation

2001 • 725 citations

Tumour-suppressor activity of H19 RNA

1993 • 638 citations

von Hippel-Lindau disease: genetic, clinical, and imaging features.

1995 • 539 citations

An inherited p53 mutation that contributes in a tissue-specific manner to pediatric adrenal cortical carcinoma

2001 • 519 citations

Pheochromocytomas, Multiple Endocrine Neoplasia Type 2, and von Hippel-Lindau Disease

1993 • 471 citations

Carney complex, a familial multiple neoplasia and lentiginosis syndrome. Analysis of 11 kindreds and linkage to the short arm of chromosome 2.

1996 • 451 citations

A linked genetic marker for multiple endocrine neoplasia type 2A on chromosome 10

1987 • 440 citations

The GDNF/RET signaling pathway and human diseases

2001 • 432 citations

Assignment of multiple endocrine neoplasia type 2A to chromosome 10 by linkage

1987 • 423 citations

Neurofibromatosis Type 2

2012 • 399 citations

VON RECKLINGHAUSEN′S DISEASE AND PHEOCHROMOCYTOMAS

1999 • 342 citations

Clustering of features of von Hippel-Lindau syndrome: evidence for a complex genetic locus

1991 • 337 citations

Multiple roles of the tumor suppressor p53

2002 • 335 citations

RET Proto-Oncogene in the Development of Human Cancer

1999 • 333 citations

Adrenal Incidentaloma: A New Cause of the Metabolic Syndrome?

2002 • 322 citations

Ectopic and Abnormal Hormone Receptors in Adrenal Cushing’s Syndrome*

2001 • 321 citations

Pheochromocytomas in von Hippel-Lindau Syndrome and Multiple Endocrine Neoplasia Type 2 Display Distinct Biochemical and Clinical Phenotypes

2001 • 293 citations

ON THE PREVALENCE OF ADRENOCORTICAL ADENOMAS IN AN AUTOPSY MATERIAL IN RELATION TO HYPERTENSION AND DIABETES

1968 • 290 citations

Molecular markers and long-term recurrences in a large cohort of patients with sporadic adrenocortical tumors.

2001 • 288 citations

Adrenocortical Carcinoma: Clinical, Morphologic, and Molecular Characterization

2002 • 288 citations

Somatic and occult germ-line mutations in SDHD, a mitochondrial complex II gene, in nonfamilial pheochromocytoma.

2000 • 281 citations

Mutations in the protein kinase A R1α regulatory subunit cause familial cardiac myxomas and Carney complex

2000 • 274 citations

Small changes in expression affect predisposition to tumorigenesis

2001 • 268 citations

A microdissection technique for archival DNA analysis of specific cell populations in lesions < 1 mm in size.

1995 • 267 citations

Macroglossia, omphalocele, adrenal cytomegaly, gigantism, and hyperplastic visceromegaly

1969 • 259 citations

CLINICAL AND GENETIC CHARACTERIZATION OF PHEOCHROMOCYTOMA IN VON HIPPEL-LINDAU FAMILIES: COMPARISON WITH SPORADIC PHEOCHROMOCYTOMA GIVES INSIGHT INTO NATURAL HISTORY OF PHEOCHROMOCYTOMA

1999 • 252 citations

Paradoxical Response to Dexamethasone in the Diagnosis of Primary Pigmented Nodular Adrenocortical Disease

1999 • 237 citations

Incidentally discovered adrenal masses

1995 • 231 citations

Adrenal incidentaloma and patients with homozygous or heterozygous congenital adrenal hyperplasia.

1992 • 225 citations

Clinical and genetic features of adrenocortical lesions in multiple endocrine neoplasia type 1.

1992 • 224 citations

Adrenal Medullary Disease in Multiple Endocrine Neoplasia, Type 2: Pheochromocytoma and Its Precursors

1976 • 220 citations

Identification of a Novel Genetic Locus for Familial Cardiac Myxomas and Carney Complex

1998 • 219 citations

High Frequency of Germline p53 Mutations in Childhood Adrenocortical Cancer

1994 • 219 citations

Somatic inactivation of the VHL gene in Von Hippel-Lindau disease tumors.

1997 • 217 citations

Structural and Functional Abnormalities at 11p15 Are Associated with the Malignant Phenotype in Sporadic Adrenocortical Tumors: Study on a Series of 82 Tumors¹

1997 • 217 citations

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)

2000 • 208 citations

Rearrangements at the 11p15 locus and overexpression of insulin-like growth factor-II gene in sporadic adrenocortical tumors.

1994 • 207 citations

p53 mutations in human adrenocortical neoplasms: immunohistochemical and molecular studies.

1994 • 205 citations

The von Hippel-Lindau Tumor Suppressor Gene

2020 • 201 citations

An Inherited Mutation Outside the Highly Conserved DNA-Binding Domain of the p53 Tumor Suppressor Protein in Children and Adults with Sporadic Adrenocortical Tumors

2001 • 200 citations

Genetic aberrations in adrenocortical tumors detected using comparative genomic hybridization correlate with tumor size and malignancy.

1996 • 196 citations

Multiple endocrine neoplasia type 1: new clinical and basic findings

2001 • 190 citations

Adrenocortical Tumors*

1997 • 188 citations

Allelic deletions of the VHL gene detected in multiple microscopic clear cell renal lesions in von Hippel-Lindau disease patients.

1996 • 187 citations

Multiple endocrine neoplasia type IIa

1985 • 172 citations

Mutations in the RET proto-oncogene and the von Hippel-Lindau disease tumour suppressor gene in sporadic and syndromic phaeochromocytomas.

1995 • 171 citations

ACTH induces up-regulation of ACTH receptor mRNA in mouse and human adrenocortical cell lines

1994 • 170 citations

PLASMA RENIN ACTIVITY IN PRIMARY ALDOSTERONISM. IMPORTANCE IN DIFFERENTIAL DIAGNOSIS AND IN RESEARCH OF ESSENTIAL HYPERTENSION.

1964 • 168 citations

Structural and Functional Abnormalities at 11p15 Are Associated with the Malignant Phenotype in Sporadic Adrenocortical Tumors: Study on a Series of 82 Tumors

1997 • 168 citations

Prevalence of pheochromocytoma and hyperparathyroidism in multiple endocrine neoplasia type 2A: results of long-term follow-up.

1993 • 166 citations

Hippel-Lindau disease: MR imaging.

1988 • 166 citations

Cushing’s syndrome caused by nodular adrenal hyperplasia in children with McCune-Albright syndrome

1999 • 163 citations

Clinical Implications of Genetic Defects in G Proteins: The Molecular Basis of McCune-Albright Syndrome and Albright Hereditary Osteodystrophy

1996 • 161 citations

SMALL ADENOMAS OF THE ADRENAL CORTEX IN HYPERTENSION AND DIABETES

1945 • 160 citations

Adrenocortical carcinoma is characterized by a high frequency of chromosomal gains and high-level amplifications

2000 • 159 citations

Loss of NF1 alleles in phaeochromocytomas from patients with type 1 neurofibromatosis

1992 • 157 citations

Molecular genetic investigations of the mechanism of tumourigenesis in von Hippel-Lindau disease: analysis of allele loss in VHL tumours

1994 • 150 citations

Adrenal Involvement in Multiple Endocrine Neoplasia Type 1

2002 • 146 citations

p53 Mutations in sporadic adrenocortical tumors

1993 • 144 citations

Insulin-like growth factors (IGFs) and their receptors in adrenal tumors: high IGF-II expression in functional adrenocortical carcinomas.

1993 • 143 citations

Adrenal medullary hyperplasia. A morphometric analysis in patients with familial medullary thyroid carcinoma.

1976 • 143 citations

C-cell hyperplasia, pheochromocytoma and sympathoadrenal malformation in a mouse model of multiple endocrine neoplasia type 2B

2000 • 143 citations

Loss of heterozygosity suggests multiple genetic alterations in pheochromocytomas and medullary thyroid carcinomas.

1991 • 140 citations

Rare mutations of the Gs alpha subunit gene in human endocrine tumors. Mutation detection by polymerase chain reaction—primer-introduced restriction analysis

1993 • 140 citations

RASSF1A promoter region CpG island hypermethylation in phaeochromocytomas and neuroblastoma tumours

2001 • 137 citations

Comparative Genomic Hybridization Analysis of Adrenocortical Tumors

2002 • 136 citations

Genetic events in tumour initiation and progression in multiple endocrine neoplasia type 2

1993 • 134 citations

Clonal composition of human adrenocortical neoplasms.

1994 • 133 citations

Prognostic markers in pheochromocytoma

1998 • 129 citations

Comparative Genomic Hybridization Analysis of Adrenocortical Tumors of Childhood¹

1999 • 119 citations

Genotyping of Adrenocortical Tumors: Very Frequent Deletions of the MEN1 Locus in 11q13 and of a 1-Centimorgan Region in 2p161

1999 • 118 citations

Consistent association of 1p loss of heterozygosity with pheochromocytomas from patients with multiple endocrine neoplasia type 2 syndromes.

1992 • 118 citations

p53 mutations in human adrenocortical neoplasms: immunohistochemical and molecular studies

1994 • 117 citations

Mutations of the p53 gene in human functional adrenal neoplasms.

1994 • 115 citations

Comparative Genomic Hybridization Reveals Frequent Losses of Chromosomes 1p and 3q in Pheochromocytomas and Abdominal Paragangliomas, Suggesting a Common Genetic Etiology

2000 • 115 citations

Losses of Chromosomes 1p and 3q Are Early Genetic Events in the Development of Sporadic Pheochromocytomas

2000 • 115 citations

Clonal analysis of human adrenocortical carcinomas and secreting adenomas

1994 • 114 citations

Plasma Renin Activity in Primary Aldosteronism

1964 • 112 citations

Molecular and Genetic Mechanisms of Tumorigenesis in Multiple Endocrine Neoplasia Type-1

2001 • 110 citations

Bilateral adrenal medullary hyperplasia in multiple endocrine neoplasia, type 2: the precursor of bilateral pheochromocytoma.

1975 • 108 citations

Analysis of Genomic Alterations in Sporadic Adrenocortical Lesions

1999 • 105 citations

No evidence for oncogenic mutations in the adrenocorticotropin receptor gene in human adrenocortical neoplasms.

1995 • 100 citations

Immunohistochemical expression of epidermal growth factor receptors in human adrenocortical carcinoma

1990 • 100 citations

Duplication of the mutant RET allele in trisomy 10 or loss of the wild-type allele in multiple endocrine neoplasia type 2-associated pheochromocytomas.

2000 • 98 citations

Diagnosis, localization, and management of pheochromocytoma pitfalls and follow-up in 41 patients

1988 • 98 citations

MEN1 Gene mutation analysis of sporadic adrenocortical lesions

1999 • 98 citations

Molecular definition of the 11p15.5 region involved in Beckwith-Wiedemann syndrome and probably in predisposition to adrenocortical carcinoma

1989 • 97 citations

Deletion of the Adrenocorticotropin Receptor Gene in Human Adrenocortical Tumors: Implications for Tumorigenesis¹

1997 • 96 citations

Molecular analysis of CDKN1C and TP53 in sporadic adrenal tumors

2001 • 95 citations

MEN1Gene Analysis in Sporadic Adrenocortical Neoplasms¹

1999 • 95 citations

Differential Genetic Alterations in von Hippel-Lindau Syndrome-Associated and Sporadic Pheochromocytomas¹

2000 • 95 citations

Clinical Implications of Genetic Defects in G Proteins

1999 • 93 citations

Limitations of size as a criterion in the evaluation of adrenal tumors

2000 • 93 citations

Differences between sporadic pheochromocytoma and pheochromocytoma in multiple endocrine neoplasia, type 2

1980 • 92 citations

Comparative Genomic Hybridization Analysis of Adrenocortical Tumors of Childhood

1999 • 92 citations

Detection of Novel Germ-line p53 Mutations in Diverse-Cancer-Prone Families Identifiled by Selecting Patients With Childhood Adrencortical Carcinoma

1992 • 92 citations

Aldosterone-secreting adrenal adenoma as part of multiple endocrine neoplasia type 1 (MEN1): loss of heterozygosity for polymorphic chromosome 11 deoxyribonucleic acid markers, including the MEN1 locus.

1992 • 89 citations

Familial hyperaldosteronism

2001 • 88 citations

Discerning malignancy in adrenocortical tumors: are molecular markers useful?

2001 • 88 citations

Germline mutations in thevhl gene in patients presenting with phaeochromocytomas

1998 • 88 citations

Cytogenetic and microsatellite alterations in tumors from patients with the syndrome of myxomas, spotty skin pigmentation, and endocrine overactivity (Carney complex).

1996 • 86 citations

Pheochromocytoma in von Hippel-Lindau Disease: Distinct Histopathologic Phenotype Compared to Pheochromocytoma in Multiple Endocrine Neoplasia Type 2

2002 • 85 citations

The Steroid Content of Adrenal Adenomas and Measurements of Aldosterone Production in Patients with Essential Hypertension and Primary Aldosteronism*

1967 • 85 citations

Clonal Origin of Inherited Medullary Thyroid Carcinoma and Pheochromocytoma

1976 • 83 citations

Multiple Endocrine Neoplasia, Type 2B

2005 • 81 citations

Bilateral occurrence of pheochromocytoma in patients with the multiple endocrine neoplasia syndrome type 2A (Sipple's syndrome)

1981 • 78 citations

Highly consistent genetic alterations in childhood adrenocortical tumours detected by comparative genomic hybridization

1999 • 78 citations

Are activating mutations of the adrenocorticotropin receptor involved in adrenal cortical neoplasia?

1995 • 77 citations

Activating mutation in the stimulatory guanine nucleotide-binding protein in an infant with Cushing's syndrome and nodular adrenal hyperplasia.

1994 • 77 citations

Loss of neurofibromin in adrenal gland tumors from patients with neurofibromatosis type I

1994 • 76 citations

Hyperplasia versus adenoma in endocrine tissues: are they different?

2002 • 74 citations

Prognostic value of p53, bcl-2, and c-erbB-2 protein expression in phaeochromocytomas

1999 • 73 citations

Deletion of the Adrenocorticotropin Receptor Gene in Human Adrenocortical Tumors: Implications for Tumorigenesis

1997 • 71 citations

Sporadic and familial pheochromocytomas are associated with loss of at least two discrete intervals on chromosome 1p.

2000 • 71 citations

Ribonucleic Acid Expression of the Clustered Imprinted Genes, p57KIP2, Insulin-Like Growth Factor II, and H19, in Adrenal Tumors and Cultured Adrenal Cells1

1997 • 69 citations

MEN1 Gene Analysis in Sporadic Adrenocortical Neoplasms

1999 • 67 citations

Familial Pheochromocytoma, Hypercalcemia, and Von Hippel-Lindau Disease

1979 • 67 citations

Differential Genetic Alterations in von Hippel-Lindau Syndrome-Associated and Sporadic Pheochromocytomas

2000 • 66 citations

A Case of Neonatal McCune‐Albright Syndrome with Cushing Syndrome and Hyperthyroidism

1991 • 65 citations

Loss of heterozygosity on the short arm of chromosomes 1 and 3 in sporadic pheochromocytoma and extra-adrenal paraganglioma

1997 • 64 citations

Elevated levels of telomerase activity in malignant pheochromocytoma

1998 • 63 citations

The RET protooncogene in sporadic pheochromocytomas: frequent MEN 2-like mutations and new molecular defects.

1995 • 63 citations

Familial Cushing's syndrome with primary adrenocortical microadenomatosis (primary adrenocortical nodular dysplasia)

1980 • 60 citations

Divergent differentiation in neuroendocrine tumors of the adrenal gland.

2000 • 60 citations

Sporadic phaeochromocytomas are rarely associated with germline mutations in the von Hippel‐Lindau and RET genes

1997 • 60 citations

Loss of neurofibromatosis type I (NFI) gene expression in pheochromocytomas from patients without NFI

1995 • 59 citations

High Expression of Cyclin E and G1 CDK and Loss of Function of p57^KIP2Are Involved in Proliferation of Malignant Sporadic Adrenocortical Tumors¹

2000 • 59 citations

Mutations in the RET protooncogene in sporadic pheochromocytomas.

1995 • 57 citations

No evidence for oncogenic mutations in guanine nucleotide-binding proteins of human adrenocortical neoplasms.

1993 • 56 citations

Clonality as Expression of Distinctive Cell Kinetics Patterns in Nodular Hyperplasias and Adenomas of the Adrenal Cortex

2000 • 56 citations

Loss of heterozygosity on the short arm of chromosome 3 in sporadic, von hippel‐lindau disease‐associated, and familial pheochromocytoma

1995 • 53 citations

Steroid 21-Hydroxylase Mutations and 21-Hydroxylase Messenger Ribonucleic Acid Expression in Human Adrenocortical Tumors1

1998 • 53 citations

Allelic losses on chromosome band 11q13 in aldosterone‐producing adrenal tumors

1995 • 52 citations

Selective loss of chromosome 11 in pheochromocytomas associated with the VHL syndrome

2002 • 52 citations

Biological characteristics of adrenocortical carcinoma: a study of p53, IGF, EGF-r, Ki-67 and PCNA in 17 adrenocortical carcinomas.

1997 • 52 citations

Mutations of K-ras oncogene in human adrenal tumours in Taiwan

1998 • 51 citations

Adrenal medullary hyperplasia.

1978 • 50 citations

Allelic imbalance of the mutant and wild-type RET allele in MEN 2A-associated medullary thyroid carcinoma

2001 • 49 citations

Transforming growth factor alpha, epidermal growth factor, and epidermal growth factor receptor expression in normal and diseased human adrenal cortex by immunohistochemistry and in situ hybridization.

1994 • 49 citations

Commentary on incidence of primary aldosteronism: current estimations based on objective data.

1969 • 46 citations

p53 mutations in adrenal tumors: Caucasian patients do not show the exon 4 "hot spot" found in Taiwan.

1996 • 46 citations

Absent Ras Gene Mutations in Human Adrenal Cortical Neoplasms and Pheochromocytomas

1993 • 46 citations

Angiotensin II type 1 receptor and ACTH receptor expression in human adrenocortical neoplasms

2001 • 45 citations

Prognostic value ofRET proto-oncogene point mutations in malignant and benign, sporadic phaeochromocytomas

1998 • 45 citations

Absence ofTP53 alterations in pheochromocytomas and medullary thyroid carcinomas

1997 • 44 citations

Telomerase activity as an indicator of potentially malignant adrenal tumors

1998 • 44 citations

Somatic Mutations of the Angiotensin II (AT₁) Receptor Gene are Not Present in Aldosterone-Producing Adenoma¹

1997 • 44 citations

Point mutations of ras genes in human adrenal cortical tumors: Absence in adrenocortical hyperplasia

1994 • 44 citations

High Expression of Cyclin E and G1 CDK and Loss of Function of p57KIP2 Are Involved in Proliferation of Malignant Sporadic Adrenocortical Tumors

2000 • 44 citations

The relatively high frequency of p53 gene mutations in multiple and malignant phaeochromocytomas

1998 • 41 citations

Regulation of Ras signaling by the cell cycle

2002 • 39 citations

The role of the insulin‐like growth factor system in adrenocortical tumourigenesis

2000 • 38 citations

Loss of Heterozygosity on Chromosomes 1p and 11p in Sporadic Pheochromocytoma

1989 • 38 citations

Telomerase Activity Is Significantly Enhanced in Malignant Adrenocortical Tumors in Comparison to Benign Adrenocortical Adenomas

2000 • 37 citations

Somatic Mutations of the Angiotensin II (AT1) Receptor Gene are Not Present in Aldosterone-Producing Adenoma

1997 • 36 citations

Survivin: a novel neuroendocrine marker for pheochromocytoma

2002 • 35 citations

Presence of a Gsα mutation in an adrenal tumor expressing LH/hCG receptors and clinically associated with Cushing's syndrome

2000 • 35 citations

Somatic VHL gene deletion and point mutation in MEN 2A-associated pheochromocytoma

2002 • 35 citations

Oncogenic mutations of α-Gi2 protein are not determinant for human adrenocortical tumourigenesis

1995 • 34 citations

No evidence for oncogenic mutations in guanine nucleotide-binding proteins of human adrenocortical neoplasms

1993 • 34 citations

Three-Decade Investigation of Familial Pheochromocytoma

1993 • 34 citations

p53 mutations in adrenal tumors: Caucasian patients do not show the exon 4 "hot spot" found in Taiwan

1996 • 33 citations

Gene Expression and Roles of Angiotensin II Type 1 and Type 2 Receptors in Human Adrenals

1998 • 33 citations

Clonal patterns in phaeochromocytomas and MEN-2A adrenal medullary hyperplasias: histological and kinetic correlates

2000 • 31 citations

A comparative study of 14 cases of familial and nonfamilial pheochromocytomas

1978 • 31 citations

Commentary on Incidence of Primary Aldosteronism

1969 • 29 citations

Inactivation of the p16 Tumor Suppressor Gene in Adrenocortical Tumors¹

1999 • 29 citations

Telomerase activity in benign and malignant adrenal tumors

2009 • 28 citations

Mutation Analysis of Gs.ALPHA., Adrenocorticotropin Receptor and p53 Genes in Japanese Patients with Adrenocortical Neoplasms. Including a Case of Gs.ALPHA. Mutation.

2000 • 28 citations

Expression and prognostic value of c‐erbB‐2 oncogene product in human phaeochromocytomas

1997 • 28 citations

Molecular and Structural Analysis of Two Novel STAR Mutations in Patients with Lipoid Congenital Adrenal Hyperplasia

2001 • 27 citations

Mapping the Human Melanocortin 2 Receptor (Adrenocorticotropic Hormone Receptor; ACTHR) Gene (MC2R) to the Small Arm of Chromosome 18 (18p11.21-pter)

1993 • 27 citations

No overrepresentation of congenital adrenal hyperplasia in patients with adrenocortical tumours

1999 • 27 citations

Steroid 21-Hydroxylase Mutations and 21-Hydroxylase Messenger Ribonucleic Acid Expression in Human Adrenocortical Tumors

1998 • 25 citations

Monoclonality of endocrine tumours: what does it mean?

2001 • 24 citations

Reassignment of the EPB4·1 gene to 1p36 and assessment of its involvement in neuroblastomas

2001 • 23 citations

Absence of angiotensin II type 1 receptor gene mutations in human adrenal tumors

1997 • 23 citations

VIRILIZING ADRENAL ADENOMA IN AN ADULT WITH THE BECKWITH‐WIEDEMANN SYNDROME: PARADOXICAL RESPONSE TO DEXAMETHASONE

1989 • 23 citations

Inactivation of the p16 Tumor Suppressor Gene in Adrenocortical Tumors

1999 • 23 citations

Multiple endocrine neoplasia type 2A

2003 • 22 citations

Deletion analysis of the p16 tumour suppressor gene in phaeochromocytomas

1996 • 22 citations

Successful laparoscopic operation of bilateral pheochromocytoma in a patient with Beckwith-Wiedemann syndrome

2002 • 22 citations

Telomerase activity in adrenal cortical tumors and pheochromocytomas with reference to clinicopathologic features

1998 • 21 citations

MEN I gene mutations in sporadic adrenal adenomas

1999 • 20 citations

Expression of c-fosand c-mycProto-Oncogenes in Human Adrenal Pheochromocytomas*

1990 • 20 citations

Beckwith-Wiedemann syndrome and virilizing cortical adrenal tumor in a child

2000 • 20 citations

Primäre pigmentierte noduläre adrenokortikale Dysplasie (PPNAD) im Rahmen des Carney-Komplexes als Ursache eines Cushing-Syndroms

2000 • 19 citations

Telomerase activity in the differentiation of benign and malignant adrenal tumors

1998 • 18 citations

Genetics of the development and function of the adrenal cortex.

2001 • 17 citations

Adrenal Medullary Hyperplasia

2018 • 16 citations

DIFFERENT ALLELIC PATTERNS AT CHROMOSOME 11q13 IN PAIRED ALDOSTERONE-PRODUCING TUMOURS AND BLOOD DNA

1996 • 16 citations

Somatic mutations of the RET proto-oncogene are not required for tumor development in multiple endocrine neoplasia type 2 (MEN 2) gene carriers.

1996 • 14 citations

Mutation analysis of the c-mos proto-oncogene and the endothelin-B receptor gene in medullary thyroid carcinoma and phaeochromocytoma

1996 • 14 citations

Complete Sequencing and mRNA Expression Analysis of the MEN-I Gene in Adrenal Myelolipoma

2000 • 13 citations

THE EFFECT OF PHYSICAL EXERCISE ON THE WEDGED AND FREE HEPATIC VENOUS PRESSURE IN NORMAL MEN

1973 • 12 citations

Adrenal ganglioneuroma

1996 • 11 citations

Multiple Endocrine Neoplasia Type 2B

2005 • 11 citations

P53 protein and its messenger ribonucleic acid in human adrenal tumors

1998 • 9 citations

[Genetics of endocrine diseases].

1979 • 9 citations

Calcium-dependent protein kinase-C activity in human adrenocortical neoplasms, hyperplastic adrenals, and normal adrenocortical tissue.

1994 • 9 citations

[112 cases of sporadic and genetically determined pheochromocytoma: a comparative pathologic study].

1999 • 7 citations

Alterations of RET, Oncogene in Human Adrenal Tumors

1998 • 6 citations

Loss of neurofibromatosis type 1 (NF1) gene expression in pheochromocytomas from patients without NF1

1994 • 6 citations

Deleted Work

1955 • 0 citations